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Doxorubicin Hydrochloride - 55390-241-10 - (Doxorubicin Hydrochloride)

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Drug Information of Doxorubicin Hydrochloride

Product NDC: 55390-241
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, POWDER, LYOPHILIZED, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Doxorubicin Hydrochloride

Product NDC: 55390-241
Labeler Name: Bedford Laboratories
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA062921
Marketing Category: ANDA
Start Marketing Date: 19960520

Package Information of Doxorubicin Hydrochloride

Package NDC: 55390-241-10
Package Description: 10 VIAL in 1 BOX (55390-241-10) > 5 mL in 1 VIAL

NDC Information of Doxorubicin Hydrochloride

NDC Code 55390-241-10
Proprietary Name Doxorubicin Hydrochloride
Package Description 10 VIAL in 1 BOX (55390-241-10) > 5 mL in 1 VIAL
Product NDC 55390-241
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Doxorubicin Hydrochloride
Dosage Form Name INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 19960520
Marketing Category Name ANDA
Labeler Name Bedford Laboratories
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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