Product NDC: | 0069-0093 |
Proprietary Name: | FLUMAZENIL |
Non Proprietary Name: | FLUMAZENIL |
Active Ingredient(s): | .1 mg/mL & nbsp; FLUMAZENIL |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0069-0093 |
Labeler Name: | Pfizer Laboratories Div Pfizer Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA078595 |
Marketing Category: | ANDA |
Start Marketing Date: | 20110510 |
Package NDC: | 0069-0093-03 |
Package Description: | 10 VIAL in 1 CARTON (0069-0093-03) > 10 mL in 1 VIAL (0069-0093-01) |
NDC Code | 0069-0093-03 |
Proprietary Name | FLUMAZENIL |
Package Description | 10 VIAL in 1 CARTON (0069-0093-03) > 10 mL in 1 VIAL (0069-0093-01) |
Product NDC | 0069-0093 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | FLUMAZENIL |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20110510 |
Marketing Category Name | ANDA |
Labeler Name | Pfizer Laboratories Div Pfizer Inc |
Substance Name | FLUMAZENIL |
Strength Number | .1 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Benzodiazepine Antagonist [EPC] |