| 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: | 66758-045-01 |
| Package Description: | 1 VIAL, SINGLE-DOSE in 1 CARTON (66758-045-01) > 1 mL in 1 VIAL, SINGLE-DOSE |
| NDC Code | 66758-045-01 |
| Proprietary Name | Vinorelbine tartrate |
| Package Description | 1 VIAL, SINGLE-DOSE in 1 CARTON (66758-045-01) > 1 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] |