Product NDC: | 64370-250 |
Proprietary Name: | VINORELBINE TARTRATE |
Non Proprietary Name: | Vinorelbine Tartrate |
Active Ingredient(s): | 10 mg/mL & nbsp; Vinorelbine Tartrate |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 64370-250 |
Labeler Name: | Pierre Fabre Medicament |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA020388 |
Marketing Category: | NDA |
Start Marketing Date: | 20110831 |
Package NDC: | 64370-250-01 |
Package Description: | 1 VIAL in 1 CARTON (64370-250-01) > 5 mL in 1 VIAL |
NDC Code | 64370-250-01 |
Proprietary Name | VINORELBINE TARTRATE |
Package Description | 1 VIAL in 1 CARTON (64370-250-01) > 5 mL in 1 VIAL |
Product NDC | 64370-250 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Vinorelbine Tartrate |
Dosage Form Name | INJECTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20110831 |
Marketing Category Name | NDA |
Labeler Name | Pierre Fabre Medicament |
Substance Name | VINORELBINE TARTRATE |
Strength Number | 10 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Vinca Alkaloid [EPC],Vinca Alkaloids [Chemical/Ingredient] |