| Product NDC: | 52584-092 |
| Proprietary Name: | Flumazenil |
| Non Proprietary Name: | Flumazenil |
| Active Ingredient(s): | .5 mg/5mL & nbsp; Flumazenil |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 52584-092 |
| Labeler Name: | General Injectables & Vaccines, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076256 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110218 |
| Package NDC: | 52584-092-10 |
| Package Description: | 1 VIAL in 1 BAG (52584-092-10) > 5 mL in 1 VIAL |
| NDC Code | 52584-092-10 |
| Proprietary Name | Flumazenil |
| Package Description | 1 VIAL in 1 BAG (52584-092-10) > 5 mL in 1 VIAL |
| Product NDC | 52584-092 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Flumazenil |
| Dosage Form Name | INJECTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20110218 |
| Marketing Category Name | ANDA |
| Labeler Name | General Injectables & Vaccines, Inc. |
| Substance Name | FLUMAZENIL |
| Strength Number | .5 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes | Benzodiazepine Antagonist [EPC] |