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] |