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epirubicin hydrochloride - 59762-5091-1 - (epirubicin hydrochloride)

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Drug Information of epirubicin hydrochloride

Product NDC: 59762-5091
Proprietary Name: epirubicin hydrochloride
Non Proprietary Name: epirubicin hydrochloride
Active Ingredient(s): 2    mg/mL & nbsp;   epirubicin hydrochloride
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of epirubicin hydrochloride

Product NDC: 59762-5091
Labeler Name: Greenstone, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050778
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 19990915

Package Information of epirubicin hydrochloride

Package NDC: 59762-5091-1
Package Description: 25 mL in 1 VIAL, SINGLE-USE (59762-5091-1)

NDC Information of epirubicin hydrochloride

NDC Code 59762-5091-1
Proprietary Name epirubicin hydrochloride
Package Description 25 mL in 1 VIAL, SINGLE-USE (59762-5091-1)
Product NDC 59762-5091
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name epirubicin hydrochloride
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 19990915
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Greenstone, LLC
Substance Name EPIRUBICIN HYDROCHLORIDE
Strength Number 2
Strength Unit mg/mL
Pharmaceutical Classes Anthracycline Topoisomerase Inhibitor [EPC],Anthracyclines [Chemical/Ingredient],Topoisomerase Inhibitors [MoA]

Complete Information of epirubicin hydrochloride


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