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DOXOrubicin Hydrochloride - 53150-317-01 - (DOXOrubicin Hydrochloride)

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Drug Information of DOXOrubicin Hydrochloride

Product NDC: 53150-317
Proprietary Name: DOXOrubicin Hydrochloride
Non Proprietary Name: DOXOrubicin Hydrochloride
Active Ingredient(s): 200    mg/100mL & nbsp;   DOXOrubicin Hydrochloride
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of DOXOrubicin Hydrochloride

Product NDC: 53150-317
Labeler Name: Amneal-Agila, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA200901
Marketing Category: ANDA
Start Marketing Date: 20130430

Package Information of DOXOrubicin Hydrochloride

Package NDC: 53150-317-01
Package Description: 1 VIAL, MULTI-DOSE in 1 CARTON (53150-317-01) > 100 mL in 1 VIAL, MULTI-DOSE

NDC Information of DOXOrubicin Hydrochloride

NDC Code 53150-317-01
Proprietary Name DOXOrubicin Hydrochloride
Package Description 1 VIAL, MULTI-DOSE in 1 CARTON (53150-317-01) > 100 mL in 1 VIAL, MULTI-DOSE
Product NDC 53150-317
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name DOXOrubicin Hydrochloride
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 20130430
Marketing Category Name ANDA
Labeler Name Amneal-Agila, LLC
Substance Name DOXORUBICIN HYDROCHLORIDE
Strength Number 200
Strength Unit mg/100mL
Pharmaceutical Classes Anthracycline Topoisomerase Inhibitor [EPC],Anthracyclines [Chemical/Ingredient],Topoisomerase Inhibitors [MoA]

Complete Information of DOXOrubicin Hydrochloride


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