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Epirubicin Hydrochloride - 61703-359-01 - (EPIRUBICIN HYDROCHLORIDE)

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Drug Information of Epirubicin Hydrochloride

Product NDC: 61703-359
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: 61703-359
Labeler Name: Hospira Worldwide, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065343
Marketing Category: ANDA
Start Marketing Date: 20070808

Package Information of Epirubicin Hydrochloride

Package NDC: 61703-359-01
Package Description: 1 VIAL, SINGLE-USE in 1 CARTON (61703-359-01) > 25 mL in 1 VIAL, SINGLE-USE

NDC Information of Epirubicin Hydrochloride

NDC Code 61703-359-01
Proprietary Name Epirubicin Hydrochloride
Package Description 1 VIAL, SINGLE-USE in 1 CARTON (61703-359-01) > 25 mL in 1 VIAL, SINGLE-USE
Product NDC 61703-359
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name EPIRUBICIN HYDROCHLORIDE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20070808
Marketing Category Name ANDA
Labeler Name Hospira Worldwide, Inc.
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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