Zanosar - 0703-4636-01 - (streptozocin)

Alphabetical Index


Drug Information of Zanosar

Product NDC: 0703-4636
Proprietary Name: Zanosar
Non Proprietary Name: streptozocin
Active Ingredient(s): 100    mg/mL & nbsp;   streptozocin
Administration Route(s): INTRAVENOUS
Dosage Form(s): POWDER, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Zanosar

Product NDC: 0703-4636
Labeler Name: Teva Parenteral Medicines, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050577
Marketing Category: NDA
Start Marketing Date: 20031203

Package Information of Zanosar

Package NDC: 0703-4636-01
Package Description: 10 mL in 1 VIAL (0703-4636-01)

NDC Information of Zanosar

NDC Code 0703-4636-01
Proprietary Name Zanosar
Package Description 10 mL in 1 VIAL (0703-4636-01)
Product NDC 0703-4636
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name streptozocin
Dosage Form Name POWDER, FOR SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20031203
Marketing Category Name NDA
Labeler Name Teva Parenteral Medicines, Inc.
Substance Name STREPTOZOCIN
Strength Number 100
Strength Unit mg/mL
Pharmaceutical Classes Alkylating Activity [MoA],Alkylating Drug [EPC]

Complete Information of Zanosar


General Information