| Product NDC: | 55390-093 |
| Proprietary Name: | Flumazenil |
| Non Proprietary Name: | Flumazenil |
| Active Ingredient(s): | .1 mg/mL & nbsp; Flumazenil |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 55390-093 |
| Labeler Name: | Bedford Laboratories |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076256 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20041011 |
| Package NDC: | 55390-093-10 |
| Package Description: | 10 VIAL, MULTI-DOSE in 1 BOX (55390-093-10) > 10 mL in 1 VIAL, MULTI-DOSE |
| NDC Code | 55390-093-10 |
| Proprietary Name | Flumazenil |
| Package Description | 10 VIAL, MULTI-DOSE in 1 BOX (55390-093-10) > 10 mL in 1 VIAL, MULTI-DOSE |
| Product NDC | 55390-093 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Flumazenil |
| Dosage Form Name | INJECTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20041011 |
| Marketing Category Name | ANDA |
| Labeler Name | Bedford Laboratories |
| Substance Name | FLUMAZENIL |
| Strength Number | .1 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Benzodiazepine Antagonist [EPC] |