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Idarubicin Hydrochloride - 0703-4156-11 - (idarubicin hydrochloride)

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Drug Information of Idarubicin Hydrochloride

Product NDC: 0703-4156
Proprietary Name: Idarubicin Hydrochloride
Non Proprietary Name: idarubicin hydrochloride
Active Ingredient(s): 1    mg/mL & nbsp;   idarubicin hydrochloride
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Idarubicin Hydrochloride

Product NDC: 0703-4156
Labeler Name: Teva Parenteral Medicines, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065036
Marketing Category: ANDA
Start Marketing Date: 20021001

Package Information of Idarubicin Hydrochloride

Package NDC: 0703-4156-11
Package Description: 1 VIAL, SINGLE-DOSE in 1 CARTON (0703-4156-11) > 20 mL in 1 VIAL, SINGLE-DOSE

NDC Information of Idarubicin Hydrochloride

NDC Code 0703-4156-11
Proprietary Name Idarubicin Hydrochloride
Package Description 1 VIAL, SINGLE-DOSE in 1 CARTON (0703-4156-11) > 20 mL in 1 VIAL, SINGLE-DOSE
Product NDC 0703-4156
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name idarubicin hydrochloride
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 20021001
Marketing Category Name ANDA
Labeler Name Teva Parenteral Medicines, Inc
Substance Name IDARUBICIN HYDROCHLORIDE
Strength Number 1
Strength Unit mg/mL
Pharmaceutical Classes Anthracycline Topoisomerase Inhibitor [EPC],Anthracyclines [Chemical/Ingredient],Topoisomerase Inhibitors [MoA]

Complete Information of Idarubicin Hydrochloride


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