Toposar - 0703-5657-01 - (Etoposide)

Alphabetical Index


Drug Information of Toposar

Product NDC: 0703-5657
Proprietary Name: Toposar
Non Proprietary Name: Etoposide
Active Ingredient(s): 20    mg/mL & nbsp;   Etoposide
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Toposar

Product NDC: 0703-5657
Labeler Name: Teva Parenteral Medicines, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074529
Marketing Category: ANDA
Start Marketing Date: 19970501

Package Information of Toposar

Package NDC: 0703-5657-01
Package Description: 1 VIAL, MULTI-DOSE in 1 CARTON (0703-5657-01) > 50 mL in 1 VIAL, MULTI-DOSE

NDC Information of Toposar

NDC Code 0703-5657-01
Proprietary Name Toposar
Package Description 1 VIAL, MULTI-DOSE in 1 CARTON (0703-5657-01) > 50 mL in 1 VIAL, MULTI-DOSE
Product NDC 0703-5657
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Etoposide
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 19970501
Marketing Category Name ANDA
Labeler Name Teva Parenteral Medicines, Inc
Substance Name ETOPOSIDE
Strength Number 20
Strength Unit mg/mL
Pharmaceutical Classes Topoisomerase Inhibitor [EPC],Topoisomerase Inhibitors [MoA]

Complete Information of Toposar


General Information