Product NDC: | 0703-4805 |
Proprietary Name: | Mesna |
Non Proprietary Name: | Mesna |
Active Ingredient(s): | 100 mg/mL & nbsp; Mesna |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0703-4805 |
Labeler Name: | Teva Parenteral Medicines, Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA075764 |
Marketing Category: | ANDA |
Start Marketing Date: | 20020501 |
Package NDC: | 0703-4805-03 |
Package Description: | 10 VIAL, MULTI-DOSE in 1 CARTON (0703-4805-03) > 10 mL in 1 VIAL, MULTI-DOSE (0703-4805-01) |
NDC Code | 0703-4805-03 |
Proprietary Name | Mesna |
Package Description | 10 VIAL, MULTI-DOSE in 1 CARTON (0703-4805-03) > 10 mL in 1 VIAL, MULTI-DOSE (0703-4805-01) |
Product NDC | 0703-4805 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Mesna |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20020501 |
Marketing Category Name | ANDA |
Labeler Name | Teva Parenteral Medicines, Inc |
Substance Name | MESNA |
Strength Number | 100 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Cytoprotective Agent [EPC] |