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Doxorubicin Hydrochloride - 0069-0170-01 - (Doxorubicin Hydrochloride)

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Drug Information of Doxorubicin Hydrochloride

Product NDC: 0069-0170
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: 0069-0170
Labeler Name: Pfizer Laboratories Div Pfizer Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA200170
Marketing Category: ANDA
Start Marketing Date: 20111029

Package Information of Doxorubicin Hydrochloride

Package NDC: 0069-0170-01
Package Description: 5 mL in 1 VIAL (0069-0170-01)

NDC Information of Doxorubicin Hydrochloride

NDC Code 0069-0170-01
Proprietary Name Doxorubicin Hydrochloride
Package Description 5 mL in 1 VIAL (0069-0170-01)
Product NDC 0069-0170
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 20111029
Marketing Category Name ANDA
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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