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] |