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Doxorubicin Hydrochloride - 47335-050-40 - (Doxorubicin Hydrochloride)

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Drug Information of Doxorubicin Hydrochloride

Product NDC: 47335-050
Proprietary Name: Doxorubicin Hydrochloride
Non Proprietary Name: Doxorubicin Hydrochloride
Active Ingredient(s): 2    mg/mL & nbsp;   Doxorubicin Hydrochloride
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTABLE, LIPOSOMAL
Coding System: National Drug Codes(NDC)

Labeler Information of Doxorubicin Hydrochloride

Product NDC: 47335-050
Labeler Name: Sun Pharma Global FZE
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA203263
Marketing Category: ANDA
Start Marketing Date: 20130205

Package Information of Doxorubicin Hydrochloride

Package NDC: 47335-050-40
Package Description: 1 VIAL, SINGLE-USE in 1 PACKAGE (47335-050-40) > 25 mL in 1 VIAL, SINGLE-USE

NDC Information of Doxorubicin Hydrochloride

NDC Code 47335-050-40
Proprietary Name Doxorubicin Hydrochloride
Package Description 1 VIAL, SINGLE-USE in 1 PACKAGE (47335-050-40) > 25 mL in 1 VIAL, SINGLE-USE
Product NDC 47335-050
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Doxorubicin Hydrochloride
Dosage Form Name INJECTABLE, LIPOSOMAL
Route Name INTRAVENOUS
Start Marketing Date 20130205
Marketing Category Name ANDA
Labeler Name Sun Pharma Global FZE
Substance Name DOXORUBICIN HYDROCHLORIDE
Strength Number 2
Strength Unit mg/mL
Pharmaceutical Classes Anthracycline Topoisomerase Inhibitor [EPC],Anthracyclines [Chemical/Ingredient],Topoisomerase Inhibitors [MoA]

Complete Information of Doxorubicin Hydrochloride


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