FLUMAZENIL - 0069-0093-03 - (FLUMAZENIL)

Alphabetical Index


Drug Information of FLUMAZENIL

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)

Labeler Information of FLUMAZENIL

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 Information of FLUMAZENIL

Package NDC: 0069-0093-03
Package Description: 10 VIAL in 1 CARTON (0069-0093-03) > 10 mL in 1 VIAL (0069-0093-01)

NDC Information of FLUMAZENIL

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]

Complete Information of FLUMAZENIL


General Information