Product NDC: | 66758-045 |
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, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 66758-045 |
Labeler Name: | Sandoz Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA078408 |
Marketing Category: | ANDA |
Start Marketing Date: | 20080213 |
Package NDC: | 66758-045-02 |
Package Description: | 1 VIAL, SINGLE-DOSE in 1 CARTON (66758-045-02) > 5 mL in 1 VIAL, SINGLE-DOSE |
NDC Code | 66758-045-02 |
Proprietary Name | Vinorelbine tartrate |
Package Description | 1 VIAL, SINGLE-DOSE in 1 CARTON (66758-045-02) > 5 mL in 1 VIAL, SINGLE-DOSE |
Product NDC | 66758-045 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Vinorelbine tartrate |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20080213 |
Marketing Category Name | ANDA |
Labeler Name | Sandoz Inc. |
Substance Name | VINORELBINE TARTRATE |
Strength Number | 10 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Vinca Alkaloid [EPC],Vinca Alkaloids [Chemical/Ingredient] |