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Idarubicin Hydrochloride - 66758-055-01 - (Idarubicin Hydrochloride)

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Drug Information of Idarubicin Hydrochloride

Product NDC: 66758-055
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: 66758-055
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091293
Marketing Category: ANDA
Start Marketing Date: 20110329

Package Information of Idarubicin Hydrochloride

Package NDC: 66758-055-01
Package Description: 5 mL in 1 VIAL, SINGLE-USE (66758-055-01)

NDC Information of Idarubicin Hydrochloride

NDC Code 66758-055-01
Proprietary Name Idarubicin Hydrochloride
Package Description 5 mL in 1 VIAL, SINGLE-USE (66758-055-01)
Product NDC 66758-055
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Idarubicin Hydrochloride
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 20110329
Marketing Category Name ANDA
Labeler Name Sandoz 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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