Drugs List

Drugs A-Z List - E
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Drugs List [Browse by brand or generic name]
E.E.S. Granules, E.E.S.-200, E.E.S.-400, E.E.S.-400 Filmtab, Eryc, EryPed, EryPed 200, EryPed 400, Ery-Tab, Erythrocin Stearate Filmtab, PCE Dispertab erythromycin (Pronunciation: er ITH roe MYE sin) - FDA

Description : Erythromycin is produced by a strain of Saccharopolyspora erythraea (formerly Streptomyces ...

  • Indications
  • To reduce the development of drug-resistant bacteria and maintain the effectiveness (erythromycin ethylsuccinate) of E.E.S. (erythromycin ethylsuccinate) and other antibac
  •   Read More
E.E.S. Granules, E.E.S.-200, E.E.S.-400, E.E.S.-400 Filmtab, Eryc, EryPed, EryPed 200, EryPed 400, Ery-Tab, Erythrocin Stearate Filmtab, PCE Dispertab erythromycin (Pronunciation: er ITH roe MYE sin) - Multum

Description : Erythromycin is produced by a strain of Saccharopolyspora erythraea (formerly Streptomyces ...

  • Indications
  • To reduce the development of drug-resistant bacteria and maintain the effectiveness (erythromycin ethylsuccinate) of E.E.S. (erythromycin ethylsuccinate) and other antibac
  •   Read More
E.E.S. Granules, E.E.S.-200, E.E.S.-400, E.E.S.-400 Filmtab, Eryc, EryPed, EryPed 200, EryPed 400, Ery-Tab, Erythrocin Stearate Filmtab, PCE Dispertab erythromycin (Pronunciation: er ITH roe MYE sin) - FDA

Description : ERY-TAB (erythromycin delayed-release tablets) is an antibacterial product containing erythromy...

  • Indications
  • To reduce the development of drug-resistant bacteria and maintain the effectiveness of ERY-TAB (erythromycin delayed release tablets) and other antibacterial drugs, ERY-
  •   Read More
E.E.S. Granules, E.E.S.-200, E.E.S.-400, E.E.S.-400 Filmtab, Eryc, EryPed, EryPed 200, EryPed 400, Ery-Tab, Erythrocin Stearate Filmtab, PCE Dispertab erythromycin (Pronunciation: er ITH roe MYE sin) - Multum

Description : ERY-TAB (erythromycin delayed-release tablets) is an antibacterial product containing erythromy...

  • Indications
  • To reduce the development of drug-resistant bacteria and maintain the effectiveness of ERY-TAB (erythromycin delayed release tablets) and other antibacterial drugs, ERY-TAB (e
  •   Read More
E.E.S. Granules, E.E.S.-200, E.E.S.-400, E.E.S.-400 Filmtab, Eryc, EryPed, EryPed 200, EryPed 400, Ery-Tab, Erythrocin Stearate Filmtab, PCE Dispertab erythromycin (Pronunciation: er ITH roe MYE sin) - FDA

Description : ERYC capsules contain enteric-coated pellets of erythromycin base for oral administration. Each...

  • Indications
  • Erythromycin is indicated in the treatment of infections caused by susceptible strains of the designated organisms in the diseases listed below: Upper respiratory tract
  •   Read More
E.E.S. Granules, E.E.S.-200, E.E.S.-400, E.E.S.-400 Filmtab, Eryc, EryPed, EryPed 200, EryPed 400, Ery-Tab, Erythrocin Stearate Filmtab, PCE Dispertab erythromycin (Pronunciation: er ITH roe MYE sin) - Multum

Description : ERYC capsules contain enteric-coated pellets of erythromycin base for oral administration. Each...

  • Indications
  • Erythromycin is indicated in the treatment of infections caused by susceptible strains of the designated organisms in the diseases listed below: Upper respiratory tract infec
  •   Read More
E.E.S. Granules, E.E.S.-200, E.E.S.-400, E.E.S.-400 Filmtab, Eryc, EryPed, EryPed 200, EryPed 400, Ery-Tab, Erythrocin Stearate Filmtab, PCE Dispertab erythromycin (Pronunciation: er ITH roe MYE sin) - FDA

Description : Erythromycin is produced by a strain of Saccharopolyspora erythraea (formerlyStreptom...

  • Indications
  • To reduce the development of drug-resistant bacteria and maintain the effectiveness of Ery-Ped and other antibacterial drugs, Ery-Ped should be used only to treat or pre
  •   Read More
E.E.S. Granules, E.E.S.-200, E.E.S.-400, E.E.S.-400 Filmtab, Eryc, EryPed, EryPed 200, EryPed 400, Ery-Tab, Erythrocin Stearate Filmtab, PCE Dispertab erythromycin (Pronunciation: er ITH roe MYE sin) - Multum

Description : ERY-TAB (erythromycin delayed-release tablets) is an antibacterial product containing erythromy...

  • Indications
  • To reduce the development of drug-resistant bacteria and maintain the effectiveness of ERY-TAB (erythromycin delayed release tablets) and other antibacterial drugs, ERY-
  •   Read More
E.E.S. Granules, E.E.S.-200, E.E.S.-400, E.E.S.-400 Filmtab, Eryc, EryPed, EryPed 200, EryPed 400, Ery-Tab, Erythrocin Stearate Filmtab, PCE Dispertab erythromycin (Pronunciation: er ITH roe MYE sin) - FDA

Description : ERYC capsules contain enteric-coated pellets of erythromycin base for oral administration. Each...

  • Indications
  • Erythromycin is indicated in the treatment of infections caused by susceptible strains of the designated organisms in the diseases listed below: Upper respiratory tract infec
  •   Read More
E.E.S. Granules, E.E.S.-200, E.E.S.-400, E.E.S.-400 Filmtab, Eryc, EryPed, EryPed 200, EryPed 400, Ery-Tab, Erythrocin Stearate Filmtab, PCE Dispertab erythromycin (Pronunciation: er ITH roe MYE sin) - Multum

Description : ERYC capsules contain enteric-coated pellets of erythromycin base for oral administration...

  • Indications
  • Erythromycin is indicated in the treatment of infections caused by susceptible strains of the designated organisms in the diseases listed below: Upper respiratory tract infec
  •   Read More
E.E.S. Granules, E.E.S.-200, E.E.S.-400, E.E.S.-400 Filmtab, Eryc, EryPed, EryPed 200, EryPed 400, Ery-Tab, Erythrocin Stearate Filmtab, PCE Dispertab erythromycin (Pronunciation: er ITH roe MYE sin) - FDA

Description : Erythromycin is produced by a strain of Saccharopolyspora erythraea (formerlyStreptom...

  • Indications
  • To reduce the development of drug-resistant bacteria and maintain the effectiveness (erythromycin ethylsuccinate) of E.E.S. (erythromycin ethylsuccinate) and other&n
  •   Read More
E.E.S. Granules, E.E.S.-200, E.E.S.-400, E.E.S.-400 Filmtab, Eryc, EryPed, EryPed 200, EryPed 400, Ery-Tab, Erythrocin Stearate Filmtab, PCE Dispertab erythromycin (Pronunciation: er ITH roe MYE sin) - Multum

Description : Erythromycin is produced by a strain of Saccharopolyspora erythraea (formerlyStreptom...

  • Indications
  • To reduce the development of drug-resistant bacteria and maintain the effectiveness (erythromycin ethylsuccinate) of E.E.S. (erythromycin ethylsuccinate) and other&n
  •   Read More
E.E.S. Granules, E.E.S.-200, E.E.S.-400, E.E.S.-400 Filmtab, Eryc, EryPed, EryPed 200, EryPed 400, Ery-Tab, Erythrocin Stearate Filmtab, PCE Dispertab erythromycin (Pronunciation: er ITH roe MYE sin) - FDA

Description : Erythromycin is produced by a strain of Saccharopolyspora erythraea (formerlyStreptom...

  • Indications
  • To reduce the development of drug-resistant bacteria and maintain the effectiveness of Ery-Ped and other antibacterial drugs, Ery-Ped should be used only to treat or prevent i
  •   Read More
E.E.S. Granules, E.E.S.-200, E.E.S.-400, E.E.S.-400 Filmtab, Eryc, EryPed, EryPed 200, EryPed 400, Ery-Tab, Erythrocin Stearate Filmtab, PCE Dispertab erythromycin (Pronunciation: er ITH roe MYE sin) - Multum

Description : Erythromycin is produced by a strain of Saccharopolyspora erythraea (formerlyStreptom...

  • Indications
  • To reduce the development of drug-resistant bacteria and maintain the effectiveness of Ery-Ped and other antibacterial drugs, Ery-Ped should be used only to treat or prevent i
  •   Read More
E.E.S. Granules, E.E.S.-200, E.E.S.-400, E.E.S.-400 Filmtab, Eryc, EryPed, EryPed 200, EryPed 400, Ery-Tab, Erythrocin Stearate Filmtab, PCE Dispertab erythromycin (Pronunciation: er ITH roe MYE sin) - FDA

Description : PCE tablets (erythromycin particles in tablets) are an antibacterial product containing special...

  • Indications
  • To reduce the development of drug-resistant bacteria and maintain the effectiveness of PCE tablets and other antibacterial drugs, PCE tablets should be use
  •   Read More
E.E.S. Granules, E.E.S.-200, E.E.S.-400, E.E.S.-400 Filmtab, Eryc, EryPed, EryPed 200, EryPed 400, Ery-Tab, Erythrocin Stearate Filmtab, PCE Dispertab erythromycin (Pronunciation: er ITH roe MYE sin) - Multum

Description : PCE tablets (erythromycin particles in tablets) are an antibacterial product containing special...

  • Indications
  • To reduce the development of drug-resistant bacteria and maintain the effectiveness of PCE tablets and other antibacterial drugs, PCE tablets should be use
  •   Read More
E.E.S. Granules, E.E.S.-200, E.E.S.-400, E.E.S.-400 Filmtab, Eryc, EryPed, EryPed 200, EryPed 400, Ery-Tab, Erythrocin Stearate Filmtab, PCE Dispertab erythromycin (Pronunciation: er ITH roe MYE sin) - FDA

Description : PCE tablets (erythromycin particles in tablets) are an antibacterial product containing spe...

  • Indications
  • To reduce the development of drug-resistant bacteria and maintain the effectiveness of PCE tablets and other antibacterial drugs, PCE tablets should be used only to treat
  •   Read More
E.E.S. Granules, E.E.S.-200, E.E.S.-400, E.E.S.-400 Filmtab, Eryc, EryPed, EryPed 200, EryPed 400, Ery-Tab, Erythrocin Stearate Filmtab, PCE Dispertab erythromycin (Pronunciation: er ITH roe MYE sin) - Multum

Description : PCE tablets (erythromycin particles in tablets) are an antibacterial product containing spe...

  • Indications
  • To reduce the development of drug-resistant bacteria and maintain the effectiveness of PCE tablets and other antibacterial drugs, PCE tablets should be used only to treat
  •   Read More
E.E.S. Granules, E.E.S.-200, E.E.S.-400, E.E.S.-400 Filmtab, Eryc, EryPed, EryPed 200, EryPed 400, Ery-Tab, Erythrocin Stearate Filmtab, PCE Dispertab Generic Name: erythromycin (Pronunciation: er ITH roe MYE sin) erythromycin (Pronunciation: er ITH roe MYE sin) - Multum

Description : Erythromycin is produced by a strain of Saccharopolyspora erythraea (formerlyStreptom...

  • Indications
  • To reduce the development of drug-resistant bacteria and maintain the effectiveness of Ery-Ped and other antibacterial drugs, Ery-Ped should be used only to treat or prevent i
  •   Read More
E.E.S. Granules, E.E.S.-200, E.E.S.-400, E.E.S.-400 Filmtab, Eryc, EryPed, EryPed 200, EryPed 400, Ery-Tab, Erythrocin Stearate Filmtab, PCE Dispertab Generic Name: erythromycin (Pronunciation: er ITH roe MYE sin) erythromycin (Pronunciation: er ITH roe MYE sin) - FDA

Description : ERY-TAB (erythromycin delayed-release tablets) is an antibacterial product containing ery...

  • Indications
  • To reduce the development of drug-resistant bacteria and maintain the effectiveness of ERY-TAB (erythromycin delayed release tablets) and other antibacterial drugs, ERY-TAB (e
  •   Read More
Econazole Nitrate Cream Econazole Nitrate Cream - FDA

Description : Econazole nitrate cream contains the antifungal agent, econazole nitrate USP 1%, in a water...

  • Indications
  • Econazole nitrate cream is indicated for topical application in the treatment of tinea pedis, tinea cruris, and tinea corporis caused by Trichophyton rubrum,Trichophyton men-t
  •   Read More
Econopred Plus, Omnipred, Pred Forte, Pred Mild, Prednisol prednisolone ophthalmic (Pronunciation: pred NIS o - Multum

Description : Omnipred (prednisolone acetate ophthalmic suspension) is an adrenocortical steroid product ...

  • Indications
  • Steroid responsive inflammatory conditions of the palpebral and bulbar conjunctiva, cornea, and anterior segment of the globe such as allergic conjunctivitis, acne rosace
  •   Read More
Econopred Plus, Omnipred, Pred Forte, Pred Mild, Prednisol  prednisolone ophthalmic (Pronunciation: pred NIS - FDA

Description : PRED FORTE® (prednisolone acetate ophthalmic suspension, USP) 1% is a topical anti-infl...

  • Indications
  • PRED FORTE® (prednisolone acetate ophthalmic suspension) is indicated for the treatment of steroid-responsive inflammation of the palpebral and bulbar conjunctiva, cornea,
  •   Read More
Econopred Plus, Omnipred, Pred Forte, Pred Mild, Prednisol prednisolone ophthalmic (Pronunciation: pred NIS o - Multum

Description : PRED FORTE® (prednisolone acetate ophthalmic suspension, USP) 1% is a topical anti-infl...

  • Indications
  • PRED FORTE® (prednisolone acetate ophthalmic suspension) is indicated for the treatment of steroid-responsive inflammation of the palpebral and bulbar conjunctiva, cornea,
  •   Read More
Econopred Plus, Omnipred, Pred Forte, Pred Mild, Prednisol prednisolone ophthalmic (Pronunciation: pred NIS o - FDA

Description : Omnipred (prednisolone acetate ophthalmic suspension) is an adrenocortical steroid product ...

  • Indications
  • Steroid responsive inflammatory conditions of the palpebral and bulbar conjunctiva, cornea, and anterior segment of the globe such as allergic conjunctivitis, acne rosacea, s
  •   Read More
Econopred Plus, Omnipred, Pred Forte, Pred Mild, Prednisol prednisolone ophthalmic (Pronunciation: pred NIS o - Multum

Description : Omnipred (prednisolone acetate ophthalmic suspension) is an adrenocortical steroid product ...

  • Indications
  • Steroid responsive inflammatory conditions of the palpebral and bulbar conjunctiva, cornea, and anterior segment of the globe such as allergic conjunctivitis, acne rosace
  •   Read More
Econopred Plus, Omnipred, Pred Forte, Pred Mild, Prednisol prednisolone ophthalmic (Pronunciation: pred NIS o - FDA

Description : PRED FORTE® (prednisolone acetate ophthalmic suspension, USP) 1% is a topical anti-infl...

  • Indications
  • PRED FORTE® (prednisolone acetate ophthalmic suspension) is indicated for the treatment of steroid-responsive inflammation of the palpebral and bulbar conjunctiva, cor
  •   Read More
Econopred Plus, Omnipred, Pred Forte, Pred Mild, Prednisol prednisolone ophthalmic (Pronunciation: pred NIS o - Multum

Description : PRED FORTE® (prednisolone acetate ophthalmic suspension, USP) 1% is a topical anti-infl...

  • Indications
  • PRED FORTE® (prednisolone acetate ophthalmic suspension) is indicated for the treatment of steroid-responsive inflammation of the palpebral and bulbar conjunctiva, cornea,
  •   Read More
Ecoza (econazole nitrate) Topical Foam - FDA

Description : Ecoza (econazole nitrate) topical foam, 1% contains the azole antifungal agent, econazole n...

  • Indications
  • Ecoza (econazole nitrate) topical foam, 1%, is indicated for the treatment of interdigital tinea pedis caused by Trichophyton rubrum, Trichophyton mentagrophytes, and Epidermo
  •   Read More
ECOZA  (econazole nitrate) Topical Foam - FDA

Description : Ecoza (econazole nitrate) topical foam, 1% contains the azole antifungal agent, econazole n...

  • Indications
  • Ecoza (econazole nitrate) topical foam, 1%, is indicated for the treatment of interdigital tinea pedis caused by Trichophyton rubrum, Trichophyton mentagrophytes, and Epidermo
  •   Read More
Edarbi azilsartan (Pronunciation: AY zil SAR tan) - FDA

Description : Edarbi (azilsartan medoxomil), a prodrug, is hydrolyzed to azilsartan in the gastrointestin...

  • Indications
  • Edarbi is an angiotensin II receptor blocker (ARB) indicated for the treatment of hypertension to lower blood pressure. Lowering blood pressure reduces the risk of fatal a
  •   Read More
Edarbi azilsartan (Pronunciation: AY zil SAR tan) - Multum

Description : Edarbi (azilsartan medoxomil), a prodrug, is hydrolyzed to azilsartan in the gastrointestin...

  • Indications
  • Edarbi is an angiotensin II receptor blocker (ARB) indicated for the treatment of hypertension to lower blood pressure. Lowering blood pressure reduces the risk of fatal a
  •   Read More
Edarbyclor  azilsartan and chlorthalidone (Pronunciation: AY - FDA

Description : Edarbyclor is a combination of azilsartan medoxomil (ARB; as its potassium salt) and chlort...

  • Indications
  • Edarbyclor contains an angiotensin II receptor blocker (ARB) and a thiazide-like diuretic and is indicated for the treatment of hypertension, to lower blood pressure. Ed
  •   Read More
Edarbyclor azilsartan and chlorthalidone (Pronunciation: AY z - FDA

Description : Edarbyclor is a combination of azilsartan medoxomil (ARB; as its potassium salt) and chlort...

  • Indications
  • Edarbyclor contains an angiotensin II receptor blocker (ARB) and a thiazide-like diuretic and is indicated for the treatment of hypertension, to lower blood pressure. Ed
  •   Read More
Edarbyclor azilsartan and chlorthalidone (Pronunciation: AY z - Multum

Description : Edarbyclor is a combination of azilsartan medoxomil (ARB; as its potassium salt) and chlort...

  • Indications
  • Edarbyclor contains an angiotensin II receptor blocker (ARB) and a thiazide-like diuretic and is indicated for the treatment of hypertension, to lower blood pressure. Ed
  •   Read More
Edecrin ethacrynic acid (Pronunciation: eth a KRIN ik AS i - FDA

Description : Ethacrynic acid is an unsaturated ketone derivative of an aryloxyacetic acid. It is designa...

  • Indications
  • EDECRIN (ethacrynic acid) is indicated for treatment of edema when an agent with greater diuretic potential than those commonly employed is required. Treatment of the e
  •   Read More
Edecrin ethacrynic acid (Pronunciation: eth a KRIN ik AS i - Multum

Description : Ethacrynic acid is an unsaturated ketone derivative of an aryloxyacetic acid. It is designa...

  • Indications
  • EDECRIN (ethacrynic acid) is indicated for treatment of edema when an agent with greater diuretic potential than those commonly employed is required. Treatment of the e
  •   Read More
Edecrin ethacrynic acid (Pronunciation: eth a KRIN ik AS i - FDA

Description : Ethacrynic acid is an unsaturated ketone derivative of an aryloxyacetic acid. It is d...

  • Indications
  • EDECRIN (ethacrynic acid) is indicated for treatment of edema when an agent with greater diuretic potential than those commonly employed is required. Tr
  •   Read More
Edecrin ethacrynic acid (Pronunciation: eth a KRIN ik AS i - Multum

Description : Ethacrynic acid is an unsaturated ketone derivative of an aryloxyacetic acid. It is d...

  • Indications
  • EDECRIN (ethacrynic acid) is indicated for treatment of edema when an agent with greater diuretic potential than those commonly employed is required. Tr
  •   Read More
Edurant rilpivirine (Pronunciation: RIL pi VIR een) - FDA

Description : EDURANT (rilpivirine) is a non-nucleoside reverse transcriptase inhibitor (NNRTI) of human ...

  • Indications
  • EDURANT® , in combination with other antiretroviral agents, is indicated for the treatment of human immunodeficiency virus type 1 (HIV-1) infection in antiretroviral t
  •   Read More
Edurant rilpivirine (Pronunciation: RIL pi VIR een) - Multum

Description : EDURANT (rilpivirine) is a non-nucleoside reverse transcriptase inhibitor (NNRTI) of human ...

  • Indications
  • EDURANT® , in combination with other antiretroviral agents, is indicated for the treatment of human immunodeficiency virus type 1 (HIV-1) infection in antiretroviral t
  •   Read More
Edurant rilpivirine (Pronunciation: RIL pi VIR een) - FDA

Description : EDURANT (rilpivirine) is a non-nucleoside reverse transcriptase inhibitor (NNRTI) of human ...

  • Indications
  • EDURANT® , in combination with other antiretroviral agents, is indicated for the treatment of human immunodeficiency virus type 1 (HIV-1) infection in antiretroviral t
  •   Read More
Edurant rilpivirine (Pronunciation: RIL pi VIR een) - Multum

Description : EDURANT (rilpivirine) is a non-nucleoside reverse transcriptase inhibitor (NNRTI) of human ...

  • Indications
  • EDURANT® , in combination with other antiretroviral agents, is indicated for the treatment of human immunodeficiency virus type 1 (HIV-1) infection in antiretroviral t
  •   Read More
EEMT (esterified estrogens and methyltestosterone) Tabl - FDA

Description : ESTERIFIED ESTROGENS AND METHYLTESTOSTERONE FULL STRENGTH: Each light green, capsule-shaped...

  • Indications
  • ESTERIFIED ESTROGENS AND METHYLTESTOSTERONE FULL STRENGTH and ESTERIFIED ESTROGENS AND METHYLTESTOSTERONE HALF STRENGTH are indicated in the treatment of: Moderate to seve
  •   Read More
EEMT (esterified estrogens and methyltestosterone) Tabl - FDA

Description : ESTERIFIED ESTROGENS AND METHYLTESTOSTERONE FULL STRENGTH: Each light green, capsule-shaped, fi...

  • Indications
  • ESTERIFIED ESTROGENS AND METHYLTESTOSTERONE FULL STRENGTH and ESTERIFIED ESTROGENS AND METHYLTESTOSTERONE HALF STRENGTH are indicated in the treatment of: Moderate to severeva
  •   Read More
Effexor, Effexor XR venlafaxine (Pronunciation: VEN la fax een) - FDA

Description : Effexor (venlafaxine hydrochloride) is a structurally novel antidepressant for oral adminis...

  • Indications
  • Effexor (venlafaxine hydrochloride) is indicated for the treatment of major depressive disorder. The efficacy of Effexor in the treatment of major depressive disorder was
  •   Read More
Effexor, Effexor XR venlafaxine (Pronunciation: VEN la fax een) - Multum

Description : Effexor (venlafaxine hydrochloride) is a structurally novel antidepressant for oral adminis...

  • Indications
  • Effexor (venlafaxine hydrochloride) is indicated for the treatment of major depressive disorder. The efficacy of Effexor in the treatment of major depressive disorder was
  •   Read More
Effexor, Effexor XR venlafaxine (Pronunciation: VEN la fax een) - FDA

Description : Effexor XR is an extended-release capsule for once-a-day oral administration that contain...

  • Indications
  • Major Depressive Disorder Effexor XR (venlafaxine hydrochloride) extended-release capsules are indicated for the treatment of major depressive disorder (MDD). Efficacy wa
  •   Read More
Effexor, Effexor XR venlafaxine (Pronunciation: VEN la fax een) - Multum

Description : Effexor XR is an extended-release capsule for once-a-day oral administration that contains ...

  • Indications
  • Major Depressive Disorder Effexor XR (venlafaxine hydrochloride) extended-release capsules are indicated for the treatment of major depressive disorder (MDD). Efficacy wa
  •   Read More
Effexor, Effexor XR venlafaxine (Pronunciation: VEN la fax een) - FDA

Description : Effexor (venlafaxine hydrochloride) is a structurally novel antidepressant for oral adminis...

  • Indications
  • Effexor (venlafaxine hydrochloride) is indicated for the treatment of major depressive disorder. The efficacy of Effexor in the treatment of major depressive disorder was
  •   Read More
Effexor, Effexor XR venlafaxine (Pronunciation: VEN la fax een) - Multum

Description : Effexor (venlafaxine hydrochloride) is a structurally novel antidepressant for oral adminis...

  • Indications
  • Effexor (venlafaxine hydrochloride) is indicated for the treatment of major depressive disorder. The efficacy of Effexor in the treatment of major depressive disorder was
  •   Read More
Effexor, Effexor XR venlafaxine (Pronunciation: VEN la fax een) - FDA

Description : Effexor XR is an extended-release capsule for once-a-day oral administration that contains ...

  • Indications
  • Major Depressive Disorder Effexor XR (venlafaxine hydrochloride) extended-release capsules are indicated for the treatment of major depressive disorder (MDD). Efficacy wa
  •   Read More
Effexor, Effexor XR venlafaxine (Pronunciation: VEN la fax een) - Multum

Description : Effexor XR is an extended-release capsule for once-a-day oral administration that contains ...

  • Indications
  • Major Depressive Disorder Effexor XR (venlafaxine hydrochloride) extended-release capsules are indicated for the treatment of major depressive disorder (MDD). Efficacy wa
  •   Read More
Effient prasugrel (Pronunciation: PRA soo grel) - FDA

Description : Effient contains prasugrel, a thienopyridine class inhibitor of platelet activation and agg...

  • Indications
  • Acute Coronary Syndrome Effient® is indicated to reduce the rate of thrombotic cardiovascular (CV) events (including stent thrombosis) in patients with acute coronary
  •   Read More
Effient prasugrel (Pronunciation: PRA soo grel - FDA

Description : Effient contains prasugrel, a thienopyridine class inhibitor of platelet activation and agg...

  • Indications
  • Acute Coronary Syndrome Effient® is indicated to reduce the rate of thrombotic cardiovascular (CV) events (including stent thrombosis) in patients with acute coronary
  •   Read More
Effient prasugrel (Pronunciation: PRA soo grel) - Multum

Description : Effient contains prasugrel, a thienopyridine class inhibitor of platelet activation and agg...

  • Indications
  • Acute Coronary Syndrome Effient® is indicated to reduce the rate of thrombotic cardiovascular (CV) events (including stent thrombosis) in patients with acute coronary
  •   Read More
Egrifta tesamorelin (Pronunciation: TES a moe REL in) - FDA

Description : EGRIFTA™ contains tesamorelin (as the acetate salt), an analog of human growth hormon...

  • Indications
  • EGRIFTA™ (tesamorelin for injection) is indicated for the reduction of excess abdominal fat in HIV-infected patients with lipodystrophy [see Clinical Studies]. Limi
  •   Read More
Egrifta tesamorelin (Pronunciation: TES a moe REL in) - Multum

Description : EGRIFTA™ contains tesamorelin (as the acetate salt), an analog of human growth hormon...

  • Indications
  • EGRIFTA™ (tesamorelin for injection) is indicated for the reduction of excess abdominal fat in HIV-infected patients with lipodystrophy [see Clinical Studies]. Limi
  •   Read More
Elaprase idursulfase (Pronunciation: EYE dur SUL fase) - FDA

Description : ELAPRASE is a formulation of idursulfase, a purified form of human iduronate-2-sulfatase, a...

  • Indications
  • ELAPRASE is indicated for patients with Hunter syndrome (Mucopolysaccharidosis II, MPS II). ELAPRASE has been shown to improve walking capacity in patients 5 years and ol
  •   Read More
Elaprase idursulfase (Pronunciation: EYE dur SUL fase) - Multum

Description : ELAPRASE is a formulation of idursulfase, a purified form of human iduronate-2-sulfatase, a...

  • Indications
  • ELAPRASE is indicated for patients with Hunter syndrome (Mucopolysaccharidosis II, MPS II). ELAPRASE has been shown to improve walking capacity in patients 5 years and ol
  •   Read More
Elaprase idursulfase (Pronunciation: EYE dur SUL fase) - FDA

Description : ELAPRASE is a formulation of idursulfase, a purified form of human iduronate-2-sulfatase, a...

  • Indications
  • ELAPRASE is indicated for patients with Hunter syndrome (Mucopolysaccharidosis II, MPS II). ELAPRASE has been shown to improve walking capacity in patients 5 years and ol
  •   Read More
Elaprase idursulfase (Pronunciation: EYE dur SUL fase) - Multum

Description : ELAPRASE is a formulation of idursulfase, a purified form of human iduronate-2-sulfatase, a...

  • Indications
  • ELAPRASE is indicated for patients with Hunter syndrome (Mucopolysaccharidosis II, MPS II). ELAPRASE has been shown to improve walking capacity in patients 5 years and ol
  •   Read More
Elavil (amitriptyline HCI) - FDA

Description : Amitriptyline HCl is 3-(10,11-dihydro-5H-dibenzo [a,d] cycloheptene-5-ylidene)-N,N-dimethyl...

  • Indications
  • For the relief of symptoms of depression. Endogenous depression is more likely to be alleviated than are other depressive states.
  •   Read More
Elavil (amitriptyline HCI) - FDA

Description : Amitriptyline HCl is 3-(10,11-dihydro-5H-dibenzo [a,d] cycloheptene-5-ylidene)-N,N-dimethyl...

  • Indications
  • For the relief of symptoms of depression. Endogenous depression is more likely to be alleviated than are other depressive states.
  •   Read More
Eldepryl, Zelapar selegiline (oral) (Pronunciation: se LE ji leen) - FDA

Description : ELDEPRYL (selegiline hydrochloride) is a levorotatory acetylenic derivative of phenethylami...

  • Indications
  • ELDEPRYL (selegiline hcl) is indicated as an adjunct in the management of Parkinsonian patients being treated with levodopa/carbidopa who exhibit deterioration in the qual
  •   Read More
Eldepryl, Zelapar selegiline (oral) (Pronunciation: se LE ji leen) - Multum

Description : ELDEPRYL (selegiline hydrochloride) is a levorotatory acetylenic derivative of phenethylami...

  • Indications
  • ELDEPRYL (selegiline hcl) is indicated as an adjunct in the management of Parkinsonian patients being treated with levodopa/carbidopa who exhibit deterioration in the qual
  •   Read More
Eldepryl, Zelapar selegiline (oral) (Pronunciation: se LE ji leen) - FDA

Description : ELDEPRYL (selegiline hydrochloride) is a levorotatory acetylenic derivative of phenethylamine. ...

  • Indications
  • ELDEPRYL (selegiline hcl) is indicated as an adjunct in the management of Parkinsonian patients being treated with levodopa/carbidopa who exhibit deterioration in the quality
  •   Read More
Eldepryl, Zelapar selegiline (oral) (Pronunciation: se LE ji leen) - Multum

Description : ELDEPRYL (selegiline hydrochloride) is a levorotatory acetylenic derivative of phenethylamine. ...

  • Indications
  • ELDEPRYL (selegiline hcl) is indicated as an adjunct in the management of Parkinsonian patients being treated with levodopa/carbidopa who exhibit deterioration in the quality
  •   Read More
Eldepryl, Zelapar selegiline (oral) (Pronunciation: se LE ji leen) - FDA

Description : ZELAPAR® Orally Disintegrating Tablets contain selegiline hydrochloride, a levorotatory ace...

  • Indications
  • ZELAPAR is indicated as an adjunct in the management of patients withParkinson's disease being treated with levodopa/carbidopa who exhibit deterioration in the quality of
  •   Read More
Eldepryl, Zelapar selegiline (oral) (Pronunciation: se LE ji leen) - Multum

Description : ZELAPAR® Orally Disintegrating Tablets contain selegiline hydrochloride, a levorotatory ace...

  • Indications
  • ZELAPAR is indicated as an adjunct in the management of patients withParkinson's disease being treated with levodopa/carbidopa who exhibit deterioration in the quality of
  •   Read More
Eldepryl, Zelapar selegiline (oral) (Pronunciation: se LE ji leen) - FDA

Description : ZELAPAR® Orally Disintegrating Tablets contain selegiline hydrochloride, a levorotatory ace...

  • Indications
  • ZELAPAR is indicated as an adjunct in the management of patients with Parkinson's disease being treated with levodopa/carbidopa who exhibit deterioration in the quality of the
  •   Read More
Eldepryl, Zelapar selegiline (oral) (Pronunciation: se LE ji leen) - FDA

Description : ZELAPAR® Orally Disintegrating Tablets contain selegiline hydrochloride, a levorotatory ace...

  • Indications
  • ZELAPAR is indicated as an adjunct in the management of patients with Parkinson's disease being treated with levodopa/carbidopa who exhibit deterioration in the quality of the
  •   Read More
Elelyso taliglucerase alfa (Pronunciation: TAL i GLOO ser - FDA

Description : Taliglucerase alfa, a hydrolytic lysosomal glucocerebroside-specific enzyme for intravenous...

  • Indications
  • ELELYSO is indicated for long-term enzyme replacement therapy (ERT) for adult and pediatric patients with a confirmed diagnosis of Type 1 Gaucher disease.
  •   Read More
Elelyso taliglucerase alfa (Pronunciation: TAL i GLOO ser - Multum

Description : Taliglucerase alfa, a hydrolytic lysosomal glucocerebroside-specific enzyme for intravenous...

  • Indications
  • ELELYSO is indicated for long-term enzyme replacement therapy (ERT) for adult and pediatric patients with a confirmed diagnosis of Type 1 Gaucher disease.
  •   Read More
Elelyso (taliglucerase alfa) Injection, for Intravenous Us - FDA

Description : Taliglucerase alfa, a hydrolytic lysosomal glucocerebroside-specific enzyme for intravenous...

  • Indications
  • ELELYSO is indicated for long-term enzyme replacement therapy (ERT) for adult and pediatric patients with a confirmed diagnosis of Type 1 Gaucher disease.
  •   Read More
Elelyso  taliglucerase alfa (Pronunciation: TAL i GLOO ser - Multum

Description : Taliglucerase alfa, a hydrolytic lysosomal glucocerebroside-specific enzyme for intravenous...

  • Indications
  • ELELYSO is indicated for long-term enzyme replacement therapy (ERT) for adult and pediatric patients with a confirmed diagnosis of Type 1 Gaucher disease.
  •   Read More
Elestat epinastine ophthalmic (Pronunciation: EP i NAS tee - FDA

Description : ELESTAT® (epinastine HCl ophthalmic solution) 0.05% is a clear, colorless, sterile isot...

  • Indications
  • ELESTAT® ophthalmic solution is indicated for the prevention of itching associated with allergic conjunctivitis.
  •   Read More
Elestat epinastine ophthalmic (Pronunciation: EP i NAS tee - Multum

Description : ELESTAT® (epinastine HCl ophthalmic solution) 0.05% is a clear, colorless, sterile isot...

  • Indications
  • ELESTAT® ophthalmic solution is indicated for the prevention of itching associated with allergic conjunctivitis.
  •   Read More
Elestat epinastine ophthalmic (Pronunciation: EP i NAS tee - FDA

Description : ELESTAT® (epinastine HCl ophthalmic solution) 0.05% is a clear, colorless, sterile isotonic...

  • Indications
  • ELESTAT® ophthalmic solution is indicated for the prevention of itchingassociated with allergic conjunctivitis.
  •   Read More
Elestat epinastine ophthalmic (Pronunciation: EP i NAS tee - Multum

Description : ELESTAT® (epinastine HCl ophthalmic solution) 0.05% is a clear, colorless, sterile isotonic...

  • Indications
  • ELESTAT® ophthalmic solution is indicated for the prevention of itchingassociated with allergic conjunctivitis.
  •   Read More
Elestrin,Divigel 0.25 mg/packet, Divigel 0.5 mg/packet, Divigel 1 mg/packet, Elestrin Pump, Estrasorb, EstroGel Pump, Evamist estradiol topical (for use on skin) (Pronunciation - FDA

Description : ELESTRIN (estradiol gel) contains 0.06% of estradiol, an estrogen, in a colorless, non-sta...

  • Indications
  • Treatment Of Moderate To Severe Vasomotor Symptoms Due To Menopause
  •   Read More
Elestrin,Divigel 0.25 mg/packet, Divigel 0.5 mg/packet, Divigel 1 mg/packet, Elestrin Pump, Estrasorb, EstroGel Pump, Evamist estradiol topical (for use on skin) (Pronunciation - Multum

Description : ELESTRIN (estradiol gel) contains 0.06% of estradiol, an estrogen, in a colorless, non-sta...

  • Indications
  • Treatment Of Moderate To Severe Vasomotor Symptoms Due To Menopause
  •   Read More
Elidel pimecrolimus topical (Pronunciation: pi MEK roe LY - FDA

Description : ELIDEL® (pimecrolimus) Cream, 1%, for topical use, contains the compound pimecrolimus, ...

  • Indications
  • ELIDEL® (pimecrolimus) Cream, 1% is indicated as second-line therapy for the short-term and non-continuous chronic treatment of mild to moderate atopic dermatitis in n
  •   Read More
Elidel pimecrolimus topical (Pronunciation: pi MEK roe LY - Multum

Description : ELIDEL® (pimecrolimus) Cream, 1%, for topical use, contains the compound pimecrolimus, ...

  • Indications
  • ELIDEL® (pimecrolimus) Cream, 1% is indicated as second-line therapy for the short-term and non-continuous chronic treatment of mild to moderate atopic dermatitis in n
  •   Read More
Elidel pimecrolimus topical (Pronunciation: pi MEK roe LY - FDA

Description : ELIDEL® (pimecrolimus) Cream, 1%, for topical use, contains the compound pimecrolimus, ...

  • Indications
  • ELIDEL® (pimecrolimus) Cream, 1% is indicated as second-line therapy for the short-term and non-continuous chronic treatment of mild to moderate atopic dermatitis in n
  •   Read More
Elidel pimecrolimus topical (Pronunciation: pi MEK roe LY - Multum

Description : ELIDEL® (pimecrolimus) Cream, 1%, for topical use, contains the compound pimecrolimus, ...

  • Indications
  • ELIDEL® (pimecrolimus) Cream, 1% is indicated as second-line therapy for the short-term and non-continuous chronic treatment of mild to moderate atopic dermatitis in n
  •   Read More
Eligard, Lupron, Lupron Depot, Lupron Depot-Ped leuprolide (Pronunciation: LOO proe lide) - FDA

Description : ELIGARD® is a sterile polymeric matrix formulation of leuprolide acetate, a GnRH agonis...

  • Indications
  • ELIGARD® is indicated for the palliative treatment of advanced prostate cancer.
  •   Read More
Eligard, Lupron, Lupron Depot, Lupron Depot-Ped leuprolide (Pronunciation: LOO proe lide) - Multum

Description : ELIGARD® is a sterile polymeric matrix formulation of leuprolide acetate, a GnRH agonis...

  • Indications
  • ELIGARD® is indicated for the palliative treatment of advanced prostate cancer.
  •   Read More
Eligard, Lupron, Lupron Depot, Lupron Depot-Ped leuprolide (Pronunciation: LOO proe lide) - FDA

Description : ELIGARD® is a sterile polymeric matrix formulation of leuprolide acetate, a GnRH agonis...

  • Indications
  • ELIGARD® is indicated for the palliative treatment of advanced prostate cancer.
  •   Read More
Eligard, Lupron, Lupron Depot, Lupron Depot-Ped leuprolide (Pronunciation: LOO proe lide) - Multum

Description : ELIGARD® is a sterile polymeric matrix formulation of leuprolide acetate, a GnRH agonis...

  • Indications
  • ELIGARD® is indicated for the palliative treatment of advanced prostate cancer.
  •   Read More
Eligard, Lupron, Lupron Depot, Lupron Depot-Ped leuprolide (Pronunciation: LOO proe lide) - FDA

Description : Leuprolide acetate is a synthetic nonapeptide analog of naturally occurring gonadotropin-re...

  • Indications
  • LUPRON DEPOT 22.5 mg for 3–month administration, 30 mg for 4–month administration, and 45 mg for 6– month administration (leuprolide acetate) are indicat
  •   Read More
Eligard, Lupron, Lupron Depot, Lupron Depot-Ped leuprolide (Pronunciation: LOO proe lide) - Multum

Description : Leuprolide acetate is a synthetic nonapeptide analog of naturally occurring gonadotropin-re...

  • Indications
  • LUPRON DEPOT 22.5 mg for 3–month administration, 30 mg for 4–month administration, and 45 mg for 6– month administration (leuprolide acetate) are indicat
  •   Read More
Eligard, Lupron, Lupron Depot, Lupron Depot-Ped leuprolide (Pronunciation: LOO proe lide) - FDA

Description : Leuprolide acetate is a synthetic nonapeptide analog of naturally occurring gonadotropin-re...

  • Indications
  • Endometriosis LUPRON DEPOT–3 Month 11.25 mg is indicated for management of endometriosis, including pain relief and reduction of endometriotic lesions. LUPRON DEPOT
  •   Read More
Eligard, Lupron, Lupron Depot, Lupron Depot-Ped leuprolide (Pronunciation: LOO proe lide) - Multum

Description : Leuprolide acetate is a synthetic nonapeptide analog of naturally occurring gonadotropin-re...

  • Indications
  • Endometriosis LUPRON DEPOT–3 Month 11.25 mg is indicated for management of endometriosis, including pain relief and reduction of endometriotic lesions. LUPRON DEPOT
  •   Read More
Eligard, Lupron, Lupron Depot, Lupron Depot-Ped leuprolide (Pronunciation: LOO proe lide) - FDA

Description : Leuprolide acetate is a synthetic nonapeptide analog of naturally occurring gonadotropin-re...

  • Indications
  • LUPRON DEPOT 7.5 mg for 1-month administration is indicated in the palliative treatment of advanced prostatic cancer.
  •   Read More
Eligard, Lupron, Lupron Depot, Lupron Depot-Ped leuprolide (Pronunciation: LOO proe lide) - Multum

Description : Leuprolide acetate is a synthetic nonapeptide analog of naturally occurring gonadotropin-re...

  • Indications
  • LUPRON DEPOT 7.5 mg for 1-month administration is indicated in the palliative treatment of advanced prostatic cancer.
  •   Read More
Eligard, Lupron, Lupron Depot, Lupron Depot-Ped leuprolide (Pronunciation: LOO proe lide) - FDA

Description : Leuprolide acetate is a synthetic nonapeptide analog of naturally occurring gonadotropin-re...

  • Indications
  • LUPRON DEPOT (leuprolide acetate for depot suspension injection) –3 Month 22.5 mg is indicated in the palliative treatment of advanced prostatic cancer. It offers an
  •   Read More
Eligard, Lupron, Lupron Depot, Lupron Depot-Ped leuprolide (Pronunciation: LOO proe lide) - Multum

Description : Leuprolide acetate is a synthetic nonapeptide analog of naturally occurring gonadotropin-re...

  • Indications
  • LUPRON DEPOT (leuprolide acetate for depot suspension injection) –3 Month 22.5 mg is indicated in the palliative treatment of advanced prostatic cancer. It offers an
  •   Read More
Eligard, Lupron, Lupron Depot, Lupron Depot-Ped leuprolide (Pronunciation: LOO proe lide) - FDA

Description : Leuprolide acetate is a synthetic nonapeptide analog of naturally occurring gonadotropin re...

  • Indications
  • LUPRON INJECTION (leuprolide acetate) is indicated in the palliative treatment of advanced prostatic cancer.
  •   Read More
Eligard, Lupron, Lupron Depot, Lupron Depot-Ped leuprolide (Pronunciation: LOO proe lide) - Multum

Description : Leuprolide acetate is a synthetic nonapeptide analog of naturally occurring gonadotropin re...

  • Indications
  • LUPRON INJECTION (leuprolide acetate) is indicated in the palliative treatment of advanced prostatic cancer.
  •   Read More
Eligard, Lupron, Lupron Depot, Lupron Depot-Ped leuprolide (Pronunciation: LOO proe lide) - FDA

Description : Leuprolide acetate is a synthetic nonapeptide analog of naturally occurring gonadotropin-re...

  • Indications
  • Endometriosis LUPRON DEPOT 3.75 mg is indicated for management of endometriosis, including pain relief and reduction of endometriotic lesions. LUPRON DEPOT monthly with
  •   Read More
Eligard, Lupron, Lupron Depot, Lupron Depot-Ped leuprolide (Pronunciation: LOO proe lide) - Multum

Description : Leuprolide acetate is a synthetic nonapeptide analog of naturally occurring gonadotropin-re...

  • Indications
  • Endometriosis LUPRON DEPOT 3.75 mg is indicated for management of endometriosis, including pain relief and reduction of endometriotic lesions. LUPRON DEPOT monthly with
  •   Read More
Eligard, Lupron, Lupron Depot, Lupron Depot-Ped leuprolide (Pronunciation: LOO proe lide) - FDA

Description : Leuprolide acetate is a synthetic nonapeptide analog of naturally occurring gonadotropin-re...

  • Indications
  • LUPRON DEPOT-PED is indicated in the treatment of children with central precocious puberty (CPP). CPP is defined as early onset of secondary sexual characteristics (gene
  •   Read More
Eligard, Lupron, Lupron Depot, Lupron Depot-Ped leuprolide (Pronunciation: LOO proe lide) - Multum

Description : Leuprolide acetate is a synthetic nonapeptide analog of naturally occurring gonadotropin-re...

  • Indications
  • LUPRON DEPOT-PED is indicated in the treatment of children with central precocious puberty (CPP). CPP is defined as early onset of secondary sexual characteristics (gene
  •   Read More
Eligard, Lupron, Lupron Depot, Lupron Depot-Ped leuprolide (Pronunciation: LOO proe lide) - FDA

Description : Leuprolide acetate is a synthetic nonapeptide analog of naturally occurring gonadotropin re...

  • Indications
  • LUPRON INJECTION (leuprolide acetate) is indicated in the palliative treatment of advanced prostatic cancer.
  •   Read More
Eligard, Lupron, Lupron Depot, Lupron Depot-Ped leuprolide (Pronunciation: LOO proe lide) - Multum

Description : Leuprolide acetate is a synthetic nonapeptide analog of naturally occurring gonadotropin re...

  • Indications
  • LUPRON INJECTION (leuprolide acetate) is indicated in the palliative treatment of advanced prostatic cancer.
  •   Read More
Eligard, Lupron, Lupron Depot, Lupron Depot-Ped leuprolide (Pronunciation: LOO proe lide) - FDA

Description : Leuprolide acetate is a synthetic nonapeptide analog of naturally occurring gonadotropin-re...

  • Indications
  • LUPRON DEPOT 22.5 mg for 3–month administration, 30 mg for 4–month administration, and 45 mg for 6– month administration (leuprolide acetate) are indicat
  •   Read More
Eligard, Lupron, Lupron Depot, Lupron Depot-Ped leuprolide (Pronunciation: LOO proe lide) - Multum

Description : Leuprolide acetate is a synthetic nonapeptide analog of naturally occurring gonadotropin-re...

  • Indications
  • LUPRON DEPOT 22.5 mg for 3–month administration, 30 mg for 4–month administration, and 45 mg for 6– month administration (leuprolide acetate) are indicat
  •   Read More
Eligard, Lupron, Lupron Depot, Lupron Depot-Ped leuprolide (Pronunciation: LOO proe lide) - FDA

Description : Leuprolide acetate is a synthetic nonapeptide analog of naturally occurring gonadotropin-re...

  • Indications
  • Endometriosis LUPRON DEPOT–3 Month 11.25 mg is indicated for management of endometriosis, including pain relief and reduction of endometriotic lesions. LUPRON DEPOT
  •   Read More
Eligard, Lupron, Lupron Depot, Lupron Depot-Ped leuprolide (Pronunciation: LOO proe lide) - Multum

Description : Leuprolide acetate is a synthetic nonapeptide analog of naturally occurring gonadotropin-re...

  • Indications
  • Endometriosis LUPRON DEPOT–3 Month 11.25 mg is indicated for management of endometriosis, including pain relief and reduction of endometriotic lesions. LUPRON DEPOT
  •   Read More
Eligard, Lupron, Lupron Depot, Lupron Depot-Ped leuprolide (Pronunciation: LOO proe lide) - FDA

Description : Leuprolide acetate is a synthetic nonapeptide analog of naturally occurring gonadotropin-re...

  • Indications
  • LUPRON DEPOT (leuprolide acetate for depot suspension injection) –3 Month 22.5 mg is indicated in the palliative treatment of advanced prostatic cancer. It offers an alt
  •   Read More
Eligard, Lupron, Lupron Depot, Lupron Depot-Ped leuprolide (Pronunciation: LOO proe lide) - Multum

Description : Leuprolide acetate is a synthetic nonapeptide analog of naturally occurring gonadotropin-re...

  • Indications
  • LUPRON DEPOT (leuprolide acetate for depot suspension injection) –3 Month 22.5 mg is indicated in the palliative treatment of advanced prostatic cancer. It offers an alt
  •   Read More
Eligard, Lupron, Lupron Depot, Lupron Depot-Ped leuprolide (Pronunciation: LOO proe lide) - FDA

Description : Leuprolide acetate is a synthetic nonapeptide analog of naturally occurring gonadotropin-re...

  • Indications
  • Endometriosis LUPRON DEPOT 3.75 mg is indicated for management of endometriosis, including pain relief and reduction of endometriotic lesions. LUPRON DEPOT monthly with
  •   Read More
Eligard, Lupron, Lupron Depot, Lupron Depot-Ped leuprolide (Pronunciation: LOO proe lide) - Multum

Description : Leuprolide acetate is a synthetic nonapeptide analog of naturally occurring gonadotropin-re...

  • Indications
  • Endometriosis LUPRON DEPOT 3.75 mg is indicated for management of endometriosis, including pain relief and reduction of endometriotic lesions. LUPRON DEPOT monthly with
  •   Read More
Eligard, Lupron, Lupron Depot, Lupron Depot-Ped leuprolide (Pronunciation: LOO proe lide) - FDA

Description : Leuprolide acetate is a synthetic nonapeptide analog of naturally occurring gonadotropin-re...

  • Indications
  • LUPRON DEPOT 7.5 mg for 1-month administration is indicated in the palliative treatment of advanced prostatic cancer.
  •   Read More
Eligard, Lupron, Lupron Depot, Lupron Depot-Ped leuprolide (Pronunciation: LOO proe lide) - Multum

Description : Leuprolide acetate is a synthetic nonapeptide analog of naturally occurring gonadotropin-re...

  • Indications
  • LUPRON DEPOT 7.5 mg for 1-month administration is indicated in the palliative treatment of advanced prostatic cancer.
  •   Read More
Eligard, Lupron, Lupron Depot, Lupron Depot-Ped leuprolide (Pronunciation: LOO proe lide) - FDA

Description : Leuprolide acetate is a synthetic nonapeptide analog of naturally occurring gonadotropin-re...

  • Indications
  • LUPRON DEPOT-PED is indicated in the treatment of children with central precocious puberty (CPP). CPP is defined as early onset of secondary sexual characteristics (gene
  •   Read More
Eligard, Lupron, Lupron Depot, Lupron Depot-Ped leuprolide (Pronunciation: LOO proe lide) - Multum

Description : Leuprolide acetate is a synthetic nonapeptide analog of naturally occurring gonadotropin-re...

  • Indications
  • LUPRON DEPOT-PED is indicated in the treatment of children with central precocious puberty (CPP). CPP is defined as early onset of secondary sexual characteristics (gene
  •   Read More
Elimite, Lice Bedding Spray, Nix Complete Lice Treatment System, Nix Cream Rinse, Nix Lice Control, RID Home Lice Control Spray for Surfaces permethrin topical (Pronunciation: per METH rin) - FDA

Description : ELIMITE® (permethrin) 5% Cream is a topical scabicidal agent for the treatment of infes...

  • Indications
  • ELIMITE® (permethrin) 5% Cream is indicated for the treatment of infestation with Sarcoptes scabiei (scabies).
  •   Read More
Elimite, Lice Bedding Spray, Nix Complete Lice Treatment System, Nix Cream Rinse, Nix Lice Control, RID Home Lice Control Spray for Surfaces permethrin topical (Pronunciation: per METH rin) - Multum

Description : ELIMITE® (permethrin) 5% Cream is a topical scabicidal agent for the treatment of infes...

  • Indications
  • ELIMITE® (permethrin) 5% Cream is indicated for the treatment of infestation with Sarcoptes scabiei (scabies).
  •   Read More
Elimite, Lice Bedding Spray, Nix Complete Lice Treatment System, Nix Cream Rinse, Nix Lice Control, RID Home Lice Control Spray for Surfaces permethrin topical (Pronunciation: per METH rin) - FDA

Description : ELIMITE® (permethrin) 5% Cream is a topical scabicidal agent for the treatment of infes...

  • Indications
  • ELIMITE® (permethrin) 5% Cream is indicated for the treatment of infestation with Sarcoptes scabiei (scabies).
  •   Read More
Elimite, Lice Bedding Spray, Nix Complete Lice Treatment System, Nix Cream Rinse, Nix Lice Control, RID Home Lice Control Spray for Surfaces permethrin topical (Pronunciation: per METH rin) - Multum

Description : ELIMITE® (permethrin) 5% Cream is a topical scabicidal agent for the treatment of infes...

  • Indications
  • ELIMITE® (permethrin) 5% Cream is indicated for the treatment of infestation with Sarcoptes scabiei (scabies).
  •   Read More
Eliphos, PhosLo Gelcap, Phoslyra calcium acetate (Pronunciation: KAL see um AH seh - FDA

Description : Each white round tablet (stamped "BRA200") contains 667 mg calcium acetate, USP (anhydrous;...

  • Indications
  • PhosLo (calcium acetate tablet) is indicated for the control of hyperphosphatemia in end stage renal failure and does not promote aluminum absorption.
  •   Read More
Eliphos, PhosLo Gelcap, Phoslyra calcium acetate (Pronunciation: KAL see um AH seh - Multum

Description : Each white round tablet (stamped "BRA200") contains 667 mg calcium acetate, USP (anhydrous;...

  • Indications
  • PhosLo (calcium acetate tablet) is indicated for the control of hyperphosphatemia in end stage renal failure and does not promote aluminum absorption.
  •   Read More
Eliphos, PhosLo Gelcap, Phoslyra calcium acetate (Pronunciation: KAL see um AH seh - FDA

Description : Each white round tablet (stamped "BRA200") contains 667 mg calcium acetate, USP (anhydrous;...

  • Indications
  • PhosLo (calcium acetate tablet) is indicated for the control of hyperphosphatemia in end stage renal failure and does not promote aluminum absorption.
  •   Read More
Eliphos, PhosLo Gelcap, Phoslyra calcium acetate (Pronunciation: KAL see um AH seh - Multum

Description : Each white round tablet (stamped "BRA200") contains 667 mg calcium acetate, USP (anhydrous;...

  • Indications
  • PhosLo (calcium acetate tablet) is indicated for the control of hyperphosphatemia in end stage renal failure and does not promote aluminum absorption.
  •   Read More
Eliquis apixaban (Pronunciation: a PIX a ban) - FDA

Description : ELIQUIS (apixaban), a factor Xa (FXa) inhibitor, is chemically described as 1-(4methoxyphen...

  • Indications
  • Reduction Of Risk Of Stroke And Systemic Embolism In Nonvalvular Atrial Fibrillation ELIQUIS® (apixaban) is indicated to reduce the risk of stroke and systemic emboli
  •   Read More
Eliquis apixaban (Pronunciation: a PIX a ban) - Multum

Description : ELIQUIS (apixaban), a factor Xa (FXa) inhibitor, is chemically described as 1-(4methoxyphen...

  • Indications
  • Reduction Of Risk Of Stroke And Systemic Embolism In Nonvalvular Atrial Fibrillation ELIQUIS® (apixaban) is indicated to reduce the risk of stroke and systemic emboli
  •   Read More
Eliquis apixaban (Pronunciation: a PIX a ban) - FDA

Description : ELIQUIS (apixaban), a factor Xa (FXa) inhibitor, is chemically described as 1-(4methoxyphen...

  • Indications
  • Reduction Of Risk Of Stroke And Systemic Embolism In Nonvalvular Atrial Fibrillation ELIQUIS® (apixaban) is indicated to reduce the risk of stroke and systemic emboli
  •   Read More
Eliquis apixaban (Pronunciation: a PIX a ban) - Multum

Description : ELIQUIS (apixaban), a factor Xa (FXa) inhibitor, is chemically described as 1-(4methoxyphen...

  • Indications
  • Reduction Of Risk Of Stroke And Systemic Embolism In Nonvalvular Atrial Fibrillation ELIQUIS® (apixaban) is indicated to reduce the risk of stroke and systemic emboli
  •   Read More
Elitek rasburicase (Pronunciation: ras BUR ih kase) - FDA

Description : Elitek (rasburicase) is a recombinant urate-oxidase produced by a genetically modified Sacc...

  • Indications
  • Elitek (rasburicase) ® is indicated for the initial management of plasma uric acid levels in pediatric and adult patients with leukemia, lymphoma, and solid tumor mali
  •   Read More
Elitek rasburicase (Pronunciation: ras BUR ih kase) - Multum

Description : Elitek (rasburicase) is a recombinant urate-oxidase produced by a genetically modified Sacc...

  • Indications
  • Elitek (rasburicase) ® is indicated for the initial management of plasma uric acid levels in pediatric and adult patients with leukemia, lymphoma, and solid tumor mali
  •   Read More
Elitek rasburicase (Pronunciation: ras BUR ih kase) - FDA

Description : Elitek (rasburicase) is a recombinant urate-oxidase produced by a genetically modified Sacc...

  • Indications
  • Elitek (rasburicase) ® is indicated for the initial management of plasma uric acid levels in pediatric and adult patients with leukemia, lymphoma, and solid tumor mali
  •   Read More
Elitek rasburicase (Pronunciation: ras BUR ih kase) - Multum

Description : Elitek (rasburicase) is a recombinant urate-oxidase produced by a genetically modified Sacc...

  • Indications
  • Elitek (rasburicase) ® is indicated for the initial management of plasma uric acid levels in pediatric and adult patients with leukemia, lymphoma, and solid tumor mali
  •   Read More
Elixophyllin, Theo-24 theophylline (Pronunciation: thee OFF i lin) - FDA

Description : Uniphyl (theophylline anhydrous tablet) ® (theophylline, anhydrous) Tablets in a contro...

  • Indications
  • Theophylline is indicated for the treatment of the symptoms and reversible airflow obstruction associated with chronic asthma and other chronic lung diseases, e.g., emphy
  •   Read More
Ella ulipristal (Pronunciation: UE li PRIS tal) - FDA

Description : The ella (ulipristal acetate) tablets for oral use contains 30 mg of a single active steroi...

  • Indications
  • ella is a progesterone agonist/antagonist emergency contraceptive indicated for prevention of pregnancy following unprotected intercourse or a known or suspected contraceptiv
  •   Read More
Ella ulipristal (Pronunciation: UE li PRIS tal) - Multum

Description : The ella (ulipristal acetate) tablets for oral use contains 30 mg of a single active steroi...

  • Indications
  • ella is a progesterone agonist/antagonist emergency contraceptive indicated for prevention of pregnancy following unprotected intercourse or a known or suspected contraceptiv
  •   Read More
Ella ulipristal (Pronunciation: UE li PRIS tal) - FDA

Description : The ella (ulipristal acetate) tablet for oral use contains 30 mg of a single active steroid...

  • Indications
  • ella is a progesterone agonist/antagonist emergency contraceptive indicated for prevention of pregnancy following unprotected intercourse or a known or suspected contraceptiv
  •   Read More
Ella ulipristal (Pronunciation: UE li PRIS tal) - Multum

Description : The ella (ulipristal acetate) tablet for oral use contains 30 mg of a single active steroid...

  • Indications
  • ella is a progesterone agonist/antagonist emergency contraceptive indicated for prevention of pregnancy following unprotected intercourse or a known or suspected contraceptiv
  •   Read More
Ellence epirubicin (Pronunciation: EP i ROO bi sin) - FDA

Description : ELLENCE Injection (epirubicin hydrochloride injection) is an anthracycline cytotoxic agent,...

  • Indications
  • ELLENCE Injection is indicated as a component of adjuvant therapy in patients with evidence of axillary node tumor involvement following resection of primary breast cancer [se
  •   Read More
Ellence epirubicin (Pronunciation: EP i ROO bi sin) - Multum

Description : ELLENCE Injection (epirubicin hydrochloride injection) is an anthracycline cytotoxic agent,...

  • Indications
  • ELLENCE Injection is indicated as a component of adjuvant therapy in patients with evidence of axillary node tumor involvement following resection of primary breast cancer [se
  •   Read More
Ellence epirubicin (Pronunciation: EP i ROO bi sin) - FDA

Description : ELLENCE Injection (epirubicin hydrochloride injection) is an anthracyclinecytotoxic agent,...

  • Indications
  • ELLENCE Injection is indicated as a component of adjuvant therapy in patients with evidence of axillary node tumor involvement following resection of prima
  •   Read More
Ellence epirubicin (Pronunciation: EP i ROO bi sin) - Multum

Description : ELLENCE Injection (epirubicin hydrochloride injection) is an anthracyclinecytotoxic agent,...

  • Indications
  • ELLENCE Injection is indicated as a component of adjuvant therapy in patients with evidence of axillary node tumor involvement following resection of prima
  •   Read More
Elmiron pentosan polysulfate sodium (Pronunciation: PEN to - FDA

Description : Pentosan polysulfate sodium is a semi-synthetically produced heparin-like macro molecular c...

  • Indications
  • ELMIRON (pentosan polysulfate sodium capsules) ® (pentosan polysulfate sodium) is indicated for the relief of bladder pain or discomfort associated with interstitial cysti
  •   Read More
Elmiron pentosan polysulfate sodium (Pronunciation: PEN to - Multum

Description : Pentosan polysulfate sodium is a semi-synthetically produced heparin-like macro molecular c...

  • Indications
  • ELMIRON (pentosan polysulfate sodium capsules) ® (pentosan polysulfate sodium) is indicated for the relief of bladder pain or discomfort associated with interstitial cysti
  •   Read More
Elmiron pentosan polysulfate sodium (Pronunciation: PEN to - FDA

Description : Pentosan polysulfate sodium is a semi-synthetically produced heparin-like macro molecular c...

  • Indications
  • ELMIRON (pentosan polysulfate sodium capsules) ® (pentosan polysulfate sodium) is indicated for the relief of bladder pain or discomfort associated with interstitial cysti
  •   Read More
Elmiron pentosan polysulfate sodium (Pronunciation: PEN to - Multum

Description : Pentosan polysulfate sodium is a semi-synthetically produced heparin-like macro molecular c...

  • Indications
  • ELMIRON (pentosan polysulfate sodium capsules) ® (pentosan polysulfate sodium) is indicated for the relief of bladder pain or discomfort associated with interstitial cysti
  •   Read More
Elocon mometasone topical (Pronunciation: moe MET a sone) - FDA

Description : ELOCON (mometasone furoate) Cream, 0.1% contains mometasone furoate for topical use. Mometasone...

  • Indications
  • ELOCON® Cream is a corticosteroid indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses in p
  •   Read More
Elocon mometasone topical (Pronunciation: moe MET a sone) - Multum

Description : ELOCON (mometasone furoate) Cream, 0.1% contains mometasone furoate for topical use. Mometasone...

  • Indications
  • ELOCON® Cream is a corticosteroid indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses in p
  •   Read More
Elocon mometasone topical (Pronunciation: moe MET a sone) - FDA

Description : ELOCON (mometasone furoate topical solution) Lotion, 0.1%, contains mometasone furoate, USP for...

  • Indications
  • ELOCON Lotion (mometasone furoate lotion) , 0.1%, is a medium potencycorticosteroid indicated for the relief of the inflammatory and pruriticmanifestations of cortic
  •   Read More
Elocon mometasone topical (Pronunciation: moe MET a sone) - Multum

Description : ELOCON (mometasone furoate topical solution) Lotion, 0.1%, contains mometasone furoate, USP for...

  • Indications
  • ELOCON Lotion (mometasone furoate lotion) , 0.1%, is a medium potencycorticosteroid indicated for the relief of the inflammatory and pruriticmanifestations of cortic
  •   Read More
Elocon mometasone topical (Pronunciation: moe MET a sone) - FDA

Description : ELOCON® (mometasone furoate) Ointment, 0.1%, contains mometasone furoate, USP for dermatolo...

  • Indications
  • ELOCON Ointment (mometasone furoate ointment) , 0.1%, is a medium potency corticosteroid indicated for the relief of the inflammatory and pruritic manifestations of
  •   Read More
Elocon mometasone topical (Pronunciation: moe MET a sone) - Multum

Description : ELOCON® (mometasone furoate) Ointment, 0.1%, contains mometasone furoate, USP for dermatolo...

  • Indications
  • ELOCON Ointment (mometasone furoate ointment) , 0.1%, is a medium potency corticosteroid indicated for the relief of the inflammatory and pruritic manifestations of
  •   Read More
Elocon mometasone topical (Pronunciation: moe MET a sone) - FDA

Description : ELOCON (mometasone furoate) Cream, 0.1% contains mometasone furoate for topical use. Mometasone...

  • Indications
  • ELOCON® Cream is a corticosteroid indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses in p
  •   Read More
Elocon mometasone topical (Pronunciation: moe MET a sone) - Multum

Description : ELOCON (mometasone furoate) Cream, 0.1% contains mometasone furoate for topical use. Mometasone...

  • Indications
  • ELOCON® Cream is a corticosteroid indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses in p
  •   Read More
Elocon mometasone topical (Pronunciation: moe MET a sone) - Multum

Description : ELOCON® (mometasone furoate) Ointment, 0.1%, contains mometasone furoate, USP for dermatolo...

  • Indications
  • ELOCON Ointment (mometasone furoate ointment) , 0.1%, is a medium potency corticosteroid indicated for the relief of the inflammatory and pruritic manifestations of
  •   Read More
Elocon Lotion,Elocon mometasone topical (Pronunciation: moe MET a sone) - FDA

Description : ELOCON (mometasone furoate topical solution) Lotion, 0.1%, contains mometasone furoate, USP for...

  • Indications
  • ELOCON Lotion (mometasone furoate lotion) , 0.1%, is a medium potencycorticosteroid indicated for the relief of the inflammatory and pruriticmanifestations of cortic
  •   Read More
Elocon Lotion,Elocon mometasone topical (Pronunciation: moe MET a sone) - Multum

Description : ELOCON (mometasone furoate topical solution) Lotion, 0.1%, contains mometasone furoate, USP for...

  • Indications
  • ELOCON Lotion (mometasone furoate lotion) , 0.1%, is a medium potencycorticosteroid indicated for the relief of the inflammatory and pruriticmanifestations of cortic
  •   Read More
Elocon Ointment,Elocon mometasone topical (Pronunciation: moe MET a sone) - FDA

Description : ELOCON® (mometasone furoate) Ointment, 0.1%, contains mometasone furoate, USP for dermatolo...

  • Indications
  • ELOCON Ointment (mometasone furoate ointment) , 0.1%, is a medium potency corticosteroid indicated for the relief of the inflammatory and pruritic manifestations of
  •   Read More
Eloctate Antihemophilic Factor (Recombinant), Fc Fusion Pro - FDA

Description : ELOCTATE, Antihemophilic Factor (Recombinant), Fc Fusion Protein, is a sterile, non-pyrogen...

  • Indications
  • ELOCTATE, Antihemophilic Factor (Recombinant), Fc Fusion Protein, is a recombinant DNA derived, antihemophilic factor indicated in adults and children with Hemophilia A (c
  •   Read More
Eloctate Antihemophilic Factor (Recombinant), Fc Fusion Pro - FDA

Description : ELOCTATE, Antihemophilic Factor (Recombinant), Fc Fusion Protein, is a sterile, non-pyrogen...

  • Indications
  • ELOCTATE, Antihemophilic Factor (Recombinant), Fc Fusion Protein, is a recombinant DNA derived, antihemophilic factor indicated in adults and children with Hemophilia A (c
  •   Read More
Eloctate [Antihemophilic Factor (Recombinant), Fc Fusion Pr - FDA

Description : ELOCTATE, Antihemophilic Factor (Recombinant), Fc Fusion Protein, is a sterile, non-pyrogenic, ...

  • Indications
  • ELOCTATE, Antihemophilic Factor (Recombinant), Fc Fusion Protein, is a recombinant DNA derived, antihemophilic factor indicated in adults and children with Hemophilia A&n
  •   Read More
Eloxatin oxaliplatin (Pronunciation: ox AL i PLA tin) - FDA

Description : ELOXATIN® (oxaliplatin injection) is an antineoplastic agent with the molecular formula C8H...

  • Indications
  • ELOXATIN, used in combination with infusional 5-fluorouracil/leucovorin, is indicated for: adjuvant treatment of stage III colon cancer in patients who have
  •   Read More
Eloxatin oxaliplatin (Pronunciation: ox AL i PLA tin) - Multum

Description : ELOXATIN® (oxaliplatin injection) is an antineoplastic agent with the molecular formula C8H...

  • Indications
  • ELOXATIN, used in combination with infusional 5-fluorouracil/leucovorin, is indicated for: adjuvant treatment of stage III colon cancer in patients who have
  •   Read More
Eloxatin oxaliplatin (Pronunciation: ox AL i PLA tin) - FDA

Description : ELOXATIN® (oxaliplatin injection) is an antineoplastic agent with the molecular formula...

  • Indications
  • ELOXATIN, used in combination with infusional 5-fluorouracil/leucovorin, is indicated for: adjuvant treatment of stage III colon cancer in patients who have undergone c
  •   Read More
Eloxatin oxaliplatin (Pronunciation: ox AL i PLA tin) - Multum

Description : ELOXATIN® (oxaliplatin injection) is an antineoplastic agent with the molecular formula...

  • Indications
  • ELOXATIN, used in combination with infusional 5-fluorouracil/leucovorin, is indicated for: adjuvant treatment of stage III colon cancer in patients who have undergone c
  •   Read More
Elspar  asparaginase (Pronunciation: as PAR a jin ase) - FDA

Description : Elspar (asparaginase) contains the enzyme L-asparagine amidohydrolase, type EC-2, derived f...

  • Indications
  • Elspar is indicated as a component of a multi-agent chemotherapeutic regimen for the treatment of patients with acute lymphoblastic leukemia (ALL).
  •   Read More
Elspar  asparaginase (Pronunciation: as PAR a jin ase) - Multum

Description : Elspar (asparaginase) contains the enzyme L-asparagine amidohydrolase, type EC-2, derived f...

  • Indications
  • Elspar is indicated as a component of a multi-agent chemotherapeutic regimen for the treatment of patients with acute lymphoblastic leukemia (ALL).
  •   Read More
Elspar asparaginase (Pronunciation: as PAR a jin ase) - FDA

Description : Elspar (asparaginase) contains the enzyme L-asparagine amidohydrolase, type EC-2, derived from&...

  • Indications
  • Elspar is indicated as a component of a multi-agent chemotherapeutic regimen for the treatment of patients with acute lymphoblastic leukemia(ALL).
  •   Read More
Elspar asparaginase (Pronunciation: as PAR a jin ase) - Multum

Description : Elspar (asparaginase) contains the enzyme L-asparagine amidohydrolase, type EC-2, derived from&...

  • Indications
  • Elspar is indicated as a component of a multi-agent chemotherapeutic regimen for the treatment of patients with acute lymphoblastic leukemia(ALL).
  •   Read More
Emadine emedastine ophthalmic (Pronunciation: EM e DAS tee - FDA

Description : EMADINE ® (emedastine difumarate ophthalmic solution) 0.05% is a sterile ophthalmic solutio...

  • Indications
  • EMADINE® (emedastine difumarate ophthalmic solution) 0.05% is indicated for the temporary relief of the signs and symptoms of allergic conjunctivitis.
  •   Read More
Emadine emedastine ophthalmic (Pronunciation: EM e DAS tee - Multum

Description : EMADINE ® (emedastine difumarate ophthalmic solution) 0.05% is a sterile ophthalmic solutio...

  • Indications
  • EMADINE® (emedastine difumarate ophthalmic solution) 0.05% is indicated for the temporary relief of the signs and symptoms of allergic conjunctivitis.
  •   Read More
Emadine emedastine ophthalmic (Pronunciation: EM e DAS tee - FDA

Description : EMADINE ® (emedastine difumarate ophthalmic solution) 0.05% is a sterile ophthalmic solutio...

  • Indications
  • EMADINE® (emedastine difumarate ophthalmic solution) 0.05% is indicated for the temporary relief of the signs and symptoms of allergic conjunctivitis.
  •   Read More
Emadine emedastine ophthalmic (Pronunciation: EM e DAS tee - Multum

Description : EMADINE ® (emedastine difumarate ophthalmic solution) 0.05% is a sterile ophthalmic solutio...

  • Indications
  • EMADINE® (emedastine difumarate ophthalmic solution) 0.05% is indicated for the temporary relief of the signs and symptoms of allergic conjunctivitis.
  •   Read More
Embeda morphine and naltrexone (Pronunciation: MOR feen a - FDA

Description : EMBEDA extended-release capsules are for oral use and contain pellets of morphine sulfate and n...

  • Indications
  • EMBEDA is indicated for the management of pain severe enough to require daily, around-the-clock, long-term opioid treatment and for which alternative treatment optio
  •   Read More
Embeda morphine and naltrexone (Pronunciation: MOR feen a - Multum

Description : EMBEDA extended-release capsules are for oral use and contain pellets of morphine sulfate and n...

  • Indications
  • EMBEDA is indicated for the management of pain severe enough to require daily, around-the-clock, long-term opioid treatment and for which alternative treatment optio
  •   Read More
Embeda morphine and naltrexone (Pronunciation: MOR feen a - FDA

Description : EMBEDA extended-release capsules are for oral use and contain pellets of morphine sulfate...

  • Indications
  • EMBEDA is indicated for the management of pain severe enough to require daily, around-the-clock, long-term opioid treatment and for which alternative treatment optio
  •   Read More
Embeda morphine and naltrexone (Pronunciation: MOR feen a - Multum

Description : EMBEDA extended-release capsules are for oral use and contain pellets of morphine sulfate and n...

  • Indications
  • EMBEDA is indicated for the management of pain severe enough to require daily, around-the-clock, long-term opioid treatment and for which alternative treatment optio
  •   Read More
Emcyt estramustine (Pronunciation: ES tra MUS teen) - FDA

Description : Estramustine phosphate sodium, an antineoplastic agent, is an off-white powder readil...

  • Indications
  • EMCYT (estramustine) Capsules are indicated in the palliative treatment of patients with metastatic and/or progressive carcinoma of the prostate.
  •   Read More
Emcyt estramustine (Pronunciation: ES tra MUS teen) - Multum

Description : Estramustine phosphate sodium, an antineoplastic agent, is an off-white powder readil...

  • Indications
  • EMCYT (estramustine) Capsules are indicated in the palliative treatment of patients with metastatic and/or progressive carcinoma of the prostate.
  •   Read More
Emcyt estramustine (Pronunciation: ES tra MUS teen) - FDA

Description : Estramustine phosphate sodium, an antineoplastic agent, is an off-white powder readil...

  • Indications
  • EMCYT (estramustine) Capsules are indicated in the palliative treatment of patients with metastatic and/or progressive carcinoma of the prostate.
  •   Read More
Emcyt estramustine (Pronunciation: ES tra MUS teen) - Multum

Description : Estramustine phosphate sodium, an antineoplastic agent, is an off-white powder readil...

  • Indications
  • EMCYT (estramustine) Capsules are indicated in the palliative treatment of patients with metastatic and/or progressive carcinoma of the prostate.
  •   Read More
Emend for Injection fosaprepitant (Pronunciation: FOS a PREP i tan t) - FDA

Description : EMEND (fosaprepitant dimeglumine) for Injection is a sterile, lyophilizedprodrug of aprepi...

  • Indications
  • EMEND® for Injection is a substance P/neurokinin-1 (NK1) receptorantagonist indicated in adults for use in combination with other antiemetic agents for the: preventi
  •   Read More
Emend for Injection fosaprepitant (Pronunciation: FOS a PREP i tan t) - Multum

Description : EMEND (fosaprepitant dimeglumine) for Injection is a sterile, lyophilizedprodrug of aprepi...

  • Indications
  • EMEND® for Injection is a substance P/neurokinin-1 (NK1) receptorantagonist indicated in adults for use in combination with other antiemetic agents for the: preventi
  •   Read More
Emend for Injection fosaprepitant (Pronunciation: FOS a PREP i tan t) - FDA

Description : EMEND (fosaprepitant dimeglumine) for Injection is a sterile, lyophilized prodrug of aprepi...

  • Indications
  • EMEND® for Injection is a substance P/neurokinin-1 (NK1) receptor antagonist indicated in adults for use in combination with other antiemetic agents for the: preventi
  •   Read More
Emend for Injection fosaprepitant (Pronunciation: FOS a PREP i tan t) - Multum

Description : EMEND (fosaprepitant dimeglumine) for Injection is a sterile, lyophilized prodrug of aprepi...

  • Indications
  • EMEND® for Injection is a substance P/neurokinin-1 (NK1) receptor antagonist indicated in adults for use in combination with other antiemetic agents for the: preventi
  •   Read More
Emend, Emend 2-Day, Emend 3-Day aprepitant (Pronunciation: a PREP i tant) - FDA

Description : EMEND (aprepitant) is a substance P/neurokinin 1 (NK1) receptor antagonist, chemically desc...

  • Indications
  • Prevention of Chemotherapy Induced Nausea and Vomiting (CINV) EMEND®, in combination with other antiemetic agents, is indicated for the: prevention of acute and de
  •   Read More
Emend, Emend 2-Day, Emend 3-Day aprepitant (Pronunciation: a PREP i tant) - Multum

Description : EMEND (aprepitant) is a substance P/neurokinin 1 (NK1) receptor antagonist, chemically desc...

  • Indications
  • Prevention of Chemotherapy Induced Nausea and Vomiting (CINV) EMEND®, in combination with other antiemetic agents, is indicated for the: prevention of acute and de
  •   Read More
Emend, Emend 2-Day, Emend 3-Day aprepitant (Pronunciation: a PREP i tant) - Multum

Description : EMEND (aprepitant) is a substance P/neurokinin 1 (NK1) receptorantagonist, chemically described...

  • Indications
  • Prevention of Chemotherapy Induced Nausea and Vomiting (CINV) EMEND®, in combination with other antiemetic agents, is indicated for the: prevention of acute and delaye
  •   Read More
Emla lidocaine and prilocaine topical (Pronunciation: L - FDA

Description : EMLA Cream (lidocaine 2.5% and prilocaine 2.5%) is an emulsion in which the oil phase is a eute...

  • Indications
  • EMLA Cream (a eutectic mixture of lidocaine 2.5% and prilocaine 2.5%) is indicated as a topical anesthetic for use on: - normal intact skin for local analgesia. -
  •   Read More
Emla lidocaine and prilocaine topical (Pronunciation: L - Multum

Description : EMLA Cream (lidocaine 2.5% and prilocaine 2.5%) is an emulsion in which the oil phase is a eute...

  • Indications
  • EMLA Cream (a eutectic mixture of lidocaine 2.5% and prilocaine 2.5%) is indicated as a topical anesthetic for use on: - normal intact skin for local analgesia. -
  •   Read More
Emla lidocaine and prilocaine topical (Pronunciation: L - FDA

Description : EMLA Cream (lidocaine 2.5% and prilocaine 2.5%) is an emulsion in which the oil phase is a ...

  • Indications
  • EMLA Cream (a eutectic mixture of lidocaine 2.5% and prilocaine 2.5%) is indicated as a topical anesthetic for use on: - normal intact skin for local analgesia. - genita
  •   Read More
Emla lidocaine and prilocaine topical (Pronunciation: L - Multum

Description : EMLA Cream (lidocaine 2.5% and prilocaine 2.5%) is an emulsion in which the oil phase is a ...

  • Indications
  • EMLA Cream (a eutectic mixture of lidocaine 2.5% and prilocaine 2.5%) is indicated as a topical anesthetic for use on: - normal intact skin for local analgesia. - genita
  •   Read More
Empirin with Codeine aspirin and codeine (Pronunciation: AS pir in and - FDA

Description : Aspirin and Codeine (acetylsalicylic acid and codeine) (WARNING: May be habit forming) As...

  • Indications
  • Aspirin and codeine phosphate tablets are indicated for the relief of mild, moderate, and moderate to severe pain
  •   Read More
Empirin with Codeine aspirin and codeine (Pronunciation: AS pir in and - Multum

Description : Aspirin and Codeine (acetylsalicylic acid and codeine) (WARNING: May be habit forming) As...

  • Indications
  • Aspirin and codeine phosphate tablets are indicated for the relief of mild, moderate, and moderate to severe pain.
  •   Read More
Empirin with Codeine aspirin and codeine (Pronunciation: AS pir in and - FDA

Description : Aspirin and Codeine(acetylsalicylic acid and codeine) (WARNING: May be habit forming) Aspirin...

  • Indications
  • Aspirin and codeine phosphate tablets are indicated for the relief of mild, moderate, and moderate to severe pain.
  •   Read More
Empirin with Codeine aspirin and codeine (Pronunciation: AS pir in and - Multum

Description : Aspirin and Codeine(acetylsalicylic acid and codeine) (WARNING: May be habit forming) Aspirin...

  • Indications
  • Aspirin and codeine phosphate tablets are indicated for the relief of mild, moderate, and moderate to severe pain.
  •   Read More
Emsam selegiline (transdermal) (Pronunciation: se LE ji - Multum

Description : EMSAM® (selegiline transdermal system) is a transdermally administered antidepressant....

  • Indications
  • EMSAM (selegiline transdermal system) is indicated for the treatment of major depressive disorder. The efficacy of EMSAM (selegiline transdermal system) in the treatment of m
  •   Read More
Emsam selegiline (transdermal) (Pronunciation: se LE ji - FDA

Description : EMSAM® (selegiline transdermal system) is a transdermally administered antidepressant....

  • Indications
  • EMSAM (selegiline transdermal system) is indicated for the treatment of major depressive disorder. The efficacy of EMSAM (selegiline transdermal system) in the treatment of m
  •   Read More
Emsam selegiline (transdermal) (Pronunciation: se LE ji - Multum

Description : EMSAM® (selegiline transdermal system) is a transdermally administered antidepressant....

  • Indications
  • EMSAM (selegiline transdermal system) is indicated for the treatment of major depressive disorder. The efficacy of EMSAM (selegiline transdermal system) in the treatment of m
  •   Read More
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