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Doxorubicin Hydrochloride - 0069-4032-01 - (DOXORUBICIN HYDROCHLORIDE)

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Drug Information of Doxorubicin Hydrochloride

Product NDC: 0069-4032
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: 0069-4032
Labeler Name: Pfizer Laboratories Div Pfizer Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050629
Marketing Category: NDA
Start Marketing Date: 20130305

Package Information of Doxorubicin Hydrochloride

Package NDC: 0069-4032-01
Package Description: 1 VIAL, SINGLE-DOSE in 1 PACKAGE (0069-4032-01) > 25 mL in 1 VIAL, SINGLE-DOSE

NDC Information of Doxorubicin Hydrochloride

NDC Code 0069-4032-01
Proprietary Name Doxorubicin Hydrochloride
Package Description 1 VIAL, SINGLE-DOSE in 1 PACKAGE (0069-4032-01) > 25 mL in 1 VIAL, SINGLE-DOSE
Product NDC 0069-4032
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name DOXORUBICIN HYDROCHLORIDE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20130305
Marketing Category Name NDA
Labeler Name Pfizer Laboratories Div Pfizer Inc
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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