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Epirubicin hydrochloride - 55390-208-01 - (Epirubicin hydrochloride)

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Drug Information of Epirubicin hydrochloride

Product NDC: 55390-208
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: 55390-208
Labeler Name: Bedford Laboratories
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065289
Marketing Category: ANDA
Start Marketing Date: 20070807

Package Information of Epirubicin hydrochloride

Package NDC: 55390-208-01
Package Description: 1 VIAL, PLASTIC in 1 BOX (55390-208-01) > 100 mL in 1 VIAL, PLASTIC

NDC Information of Epirubicin hydrochloride

NDC Code 55390-208-01
Proprietary Name Epirubicin hydrochloride
Package Description 1 VIAL, PLASTIC in 1 BOX (55390-208-01) > 100 mL in 1 VIAL, PLASTIC
Product NDC 55390-208
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Epirubicin hydrochloride
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20070807
Marketing Category Name ANDA
Labeler Name Bedford Laboratories
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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