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Vinorelbine Tartrate
Vinorelbine Tartrate - 61703-341-06 - (VINORELBINE TARTRATE)
Drug Information of Vinorelbine Tartrate
| Product NDC: | 61703-341 |
| 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) |
Labeler Information of Vinorelbine Tartrate
| Product NDC: | 61703-341 |
| Labeler Name: | Hospira Worldwide, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076827 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20050602 |
Package Information of Vinorelbine Tartrate
| Package NDC: | 61703-341-06 |
| Package Description: | 1 VIAL, SINGLE-USE in 1 CARTON (61703-341-06) > 1 mL in 1 VIAL, SINGLE-USE |
NDC Information of Vinorelbine Tartrate
| NDC Code | 61703-341-06 |
| Proprietary Name | Vinorelbine Tartrate |
| Package Description | 1 VIAL, SINGLE-USE in 1 CARTON (61703-341-06) > 1 mL in 1 VIAL, SINGLE-USE |
| Product NDC | 61703-341 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | VINORELBINE TARTRATE |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20050602 |
| Marketing Category Name | ANDA |
| Labeler Name | Hospira Worldwide, Inc. |
| Substance Name | VINORELBINE TARTRATE |
| Strength Number | 10 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Vinca Alkaloid [EPC],Vinca Alkaloids [Chemical/Ingredient] |
