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Vinblastine Sulfate
Vinblastine Sulfate - 63323-278-10 - (VINBLASTINE SULFATE)
Drug Information of Vinblastine Sulfate
| Product NDC: | 63323-278 |
| Proprietary Name: | Vinblastine Sulfate |
| Non Proprietary Name: | VINBLASTINE SULFATE |
| Active Ingredient(s): | 1 mg/mL & nbsp; VINBLASTINE SULFATE |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Vinblastine Sulfate
| Product NDC: | 63323-278 |
| Labeler Name: | APP Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA089515 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20000712 |
Package Information of Vinblastine Sulfate
| Package NDC: | 63323-278-10 |
| Package Description: | 1 VIAL, MULTI-DOSE in 1 BOX (63323-278-10) > 10 mL in 1 VIAL, MULTI-DOSE |
NDC Information of Vinblastine Sulfate
| NDC Code | 63323-278-10 |
| Proprietary Name | Vinblastine Sulfate |
| Package Description | 1 VIAL, MULTI-DOSE in 1 BOX (63323-278-10) > 10 mL in 1 VIAL, MULTI-DOSE |
| Product NDC | 63323-278 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | VINBLASTINE SULFATE |
| Dosage Form Name | INJECTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20000712 |
| Marketing Category Name | ANDA |
| Labeler Name | APP Pharmaceuticals, LLC |
| Substance Name | VINBLASTINE SULFATE |
| Strength Number | 1 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Vinca Alkaloid [EPC],Vinca Alkaloids [Chemical/Ingredient] |
