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Dacarbazine - 0703-5075-03 - (Dacarbazine)

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Drug Information of Dacarbazine

Product NDC: 0703-5075
Proprietary Name: Dacarbazine
Non Proprietary Name: Dacarbazine
Active Ingredient(s): 200    mg/20mL & nbsp;   Dacarbazine
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Dacarbazine

Product NDC: 0703-5075
Labeler Name: Teva Parenteral Medicines, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075259
Marketing Category: ANDA
Start Marketing Date: 19980827

Package Information of Dacarbazine

Package NDC: 0703-5075-03
Package Description: 10 VIAL in 1 TRAY (0703-5075-03) > 20 mL in 1 VIAL

NDC Information of Dacarbazine

NDC Code 0703-5075-03
Proprietary Name Dacarbazine
Package Description 10 VIAL in 1 TRAY (0703-5075-03) > 20 mL in 1 VIAL
Product NDC 0703-5075
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Dacarbazine
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 19980827
Marketing Category Name ANDA
Labeler Name Teva Parenteral Medicines, Inc
Substance Name DACARBAZINE
Strength Number 200
Strength Unit mg/20mL
Pharmaceutical Classes Alkylating Activity [MoA],Alkylating Drug [EPC]

Complete Information of Dacarbazine


General Information