Home > National Drug Code (NDC) > Doxorubicin Hydrochloride

Doxorubicin Hydrochloride - 0703-5046-01 - (doxorubicin hydrochloride)

Alphabetical Index


Drug Information of Doxorubicin Hydrochloride

Product NDC: 0703-5046
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
Coding System: National Drug Codes(NDC)

Labeler Information of Doxorubicin Hydrochloride

Product NDC: 0703-5046
Labeler Name: Teva Parenteral Medicines, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA064140
Marketing Category: ANDA
Start Marketing Date: 19950901

Package Information of Doxorubicin Hydrochloride

Package NDC: 0703-5046-01
Package Description: 1 VIAL, SINGLE-DOSE in 1 CARTON (0703-5046-01) > 25 mL in 1 VIAL, SINGLE-DOSE

NDC Information of Doxorubicin Hydrochloride

NDC Code 0703-5046-01
Proprietary Name Doxorubicin Hydrochloride
Package Description 1 VIAL, SINGLE-DOSE in 1 CARTON (0703-5046-01) > 25 mL in 1 VIAL, SINGLE-DOSE
Product NDC 0703-5046
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name doxorubicin hydrochloride
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 19950901
Marketing Category Name ANDA
Labeler Name Teva Parenteral Medicines, 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


General Information