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daunorubicin hydrochloride - 0703-5233-93 - (daunorubicin hydrochloride)

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Drug Information of daunorubicin hydrochloride

Product NDC: 0703-5233
Proprietary Name: daunorubicin hydrochloride
Non Proprietary Name: daunorubicin hydrochloride
Active Ingredient(s): 5    mg/mL & nbsp;   daunorubicin hydrochloride
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of daunorubicin hydrochloride

Product NDC: 0703-5233
Labeler Name: Teva Parenteral Medicines, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065035
Marketing Category: ANDA
Start Marketing Date: 20040401

Package Information of daunorubicin hydrochloride

Package NDC: 0703-5233-93
Package Description: 10 VIAL, SINGLE-DOSE in 1 TRAY (0703-5233-93) > 4 mL in 1 VIAL, SINGLE-DOSE (0703-5233-91)

NDC Information of daunorubicin hydrochloride

NDC Code 0703-5233-93
Proprietary Name daunorubicin hydrochloride
Package Description 10 VIAL, SINGLE-DOSE in 1 TRAY (0703-5233-93) > 4 mL in 1 VIAL, SINGLE-DOSE (0703-5233-91)
Product NDC 0703-5233
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name daunorubicin hydrochloride
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20040401
Marketing Category Name ANDA
Labeler Name Teva Parenteral Medicines, Inc.
Substance Name DAUNORUBICIN HYDROCHLORIDE
Strength Number 5
Strength Unit mg/mL
Pharmaceutical Classes Anthracycline Topoisomerase Inhibitor [EPC],Anthracyclines [Chemical/Ingredient],Topoisomerase Inhibitors [MoA]

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