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Epirubicin Hydrochloride - 66758-042-01 - (Epirubicin Hydrochloride)

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Drug Information of Epirubicin Hydrochloride

Product NDC: 66758-042
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: 66758-042
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065339
Marketing Category: ANDA
Start Marketing Date: 20091222

Package Information of Epirubicin Hydrochloride

Package NDC: 66758-042-01
Package Description: 1 VIAL, SINGLE-USE in 1 CARTON (66758-042-01) > 25 mL in 1 VIAL, SINGLE-USE

NDC Information of Epirubicin Hydrochloride

NDC Code 66758-042-01
Proprietary Name Epirubicin Hydrochloride
Package Description 1 VIAL, SINGLE-USE in 1 CARTON (66758-042-01) > 25 mL in 1 VIAL, SINGLE-USE
Product NDC 66758-042
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Epirubicin Hydrochloride
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20091222
Marketing Category Name ANDA
Labeler Name Sandoz 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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