Flumazenil - 63323-424-05 - (FLUMAZENIL)

Alphabetical Index


Drug Information of Flumazenil

Product NDC: 63323-424
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: 63323-424
Labeler Name: APP Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076955
Marketing Category: ANDA
Start Marketing Date: 20050405

Package Information of Flumazenil

Package NDC: 63323-424-05
Package Description: 10 VIAL, MULTI-DOSE in 1 TRAY (63323-424-05) > 5 mL in 1 VIAL, MULTI-DOSE

NDC Information of Flumazenil

NDC Code 63323-424-05
Proprietary Name Flumazenil
Package Description 10 VIAL, MULTI-DOSE in 1 TRAY (63323-424-05) > 5 mL in 1 VIAL, MULTI-DOSE
Product NDC 63323-424
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name FLUMAZENIL
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20050405
Marketing Category Name ANDA
Labeler Name APP Pharmaceuticals, LLC
Substance Name FLUMAZENIL
Strength Number .1
Strength Unit mg/mL
Pharmaceutical Classes Benzodiazepine Antagonist [EPC]

Complete Information of Flumazenil


General Information