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Vinorelbine
Vinorelbine - 0069-0099-01 - (Vinorelbine)
Drug Information of Vinorelbine
| Product NDC: | 0069-0099 |
| Proprietary Name: | Vinorelbine |
| Non Proprietary Name: | Vinorelbine |
| Active Ingredient(s): | 10 mg/mL & nbsp; Vinorelbine |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Vinorelbine
| Product NDC: | 0069-0099 |
| Labeler Name: | Pfizer Laboratories Div Pfizer Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA200148 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120901 |
Package Information of Vinorelbine
| Package NDC: | 0069-0099-01 |
| Package Description: | 1 mL in 1 VIAL (0069-0099-01) |
NDC Information of Vinorelbine
| NDC Code | 0069-0099-01 |
| Proprietary Name | Vinorelbine |
| Package Description | 1 mL in 1 VIAL (0069-0099-01) |
| Product NDC | 0069-0099 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Vinorelbine |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20120901 |
| Marketing Category Name | ANDA |
| Labeler Name | Pfizer Laboratories Div Pfizer Inc. |
| Substance Name | VINORELBINE TARTRATE |
| Strength Number | 10 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Vinca Alkaloid [EPC],Vinca Alkaloids [Chemical/Ingredient] |
