| Product NDC: | 55390-091 |
| Proprietary Name: | Vinblastine Sulfate |
| Non Proprietary Name: | Vinblastine Sulfate |
| Active Ingredient(s): | 10 mg/10mL & nbsp; Vinblastine Sulfate |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 55390-091 |
| Labeler Name: | Bedford Laboratories |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA089395 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19960501 |
| Package NDC: | 55390-091-10 |
| Package Description: | 10 VIAL in 1 BOX (55390-091-10) > 10 mL in 1 VIAL |
| NDC Code | 55390-091-10 |
| Proprietary Name | Vinblastine Sulfate |
| Package Description | 10 VIAL in 1 BOX (55390-091-10) > 10 mL in 1 VIAL |
| Product NDC | 55390-091 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Vinblastine Sulfate |
| Dosage Form Name | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 19960501 |
| Marketing Category Name | ANDA |
| Labeler Name | Bedford Laboratories |
| Substance Name | VINBLASTINE SULFATE |
| Strength Number | 10 |
| Strength Unit | mg/10mL |
| Pharmaceutical Classes | Vinca Alkaloid [EPC],Vinca Alkaloids [Chemical/Ingredient] |