Flumazenil - 25021-600-10 - (flumazenil)

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Drug Information of Flumazenil

Product NDC: 25021-600
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: 25021-600
Labeler Name: Sagent Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090584
Marketing Category: ANDA
Start Marketing Date: 20120915

Package Information of Flumazenil

Package NDC: 25021-600-10
Package Description: 10 VIAL in 1 CARTON (25021-600-10) > 10 mL in 1 VIAL

NDC Information of Flumazenil

NDC Code 25021-600-10
Proprietary Name Flumazenil
Package Description 10 VIAL in 1 CARTON (25021-600-10) > 10 mL in 1 VIAL
Product NDC 25021-600
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name flumazenil
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20120915
Marketing Category Name ANDA
Labeler Name Sagent Pharmaceuticals
Substance Name FLUMAZENIL
Strength Number .1
Strength Unit mg/mL
Pharmaceutical Classes Benzodiazepine Antagonist [EPC]

Complete Information of Flumazenil


General Information