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DOXOrubicin Hydrochloride - 62756-827-40 - (DOXOrubicin Hydrochloride)

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Drug Information of DOXOrubicin Hydrochloride

Product NDC: 62756-827
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): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of DOXOrubicin Hydrochloride

Product NDC: 62756-827
Labeler Name: Sun Pharmaceutical Industries Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091418
Marketing Category: ANDA
Start Marketing Date: 20120220

Package Information of DOXOrubicin Hydrochloride

Package NDC: 62756-827-40
Package Description: 1 VIAL, MULTI-DOSE in 1 BOX (62756-827-40) > 100 mL in 1 VIAL, MULTI-DOSE

NDC Information of DOXOrubicin Hydrochloride

NDC Code 62756-827-40
Proprietary Name DOXOrubicin Hydrochloride
Package Description 1 VIAL, MULTI-DOSE in 1 BOX (62756-827-40) > 100 mL in 1 VIAL, MULTI-DOSE
Product NDC 62756-827
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name DOXOrubicin Hydrochloride
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20120220
Marketing Category Name ANDA
Labeler Name Sun Pharmaceutical Industries Limited
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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