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Enalaprilat - 0409-2122-13 - (ENALAPRILAT)

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Drug Information of Enalaprilat

Product NDC: 0409-2122
Proprietary Name: Enalaprilat
Non Proprietary Name: ENALAPRILAT
Active Ingredient(s): 1.25    mg/mL & nbsp;   ENALAPRILAT
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Enalaprilat

Product NDC: 0409-2122
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075458
Marketing Category: ANDA
Start Marketing Date: 20090915

Package Information of Enalaprilat

Package NDC: 0409-2122-13
Package Description: 1 VIAL in 1 CARTON (0409-2122-13) > 1 mL in 1 VIAL

NDC Information of Enalaprilat

NDC Code 0409-2122-13
Proprietary Name Enalaprilat
Package Description 1 VIAL in 1 CARTON (0409-2122-13) > 1 mL in 1 VIAL
Product NDC 0409-2122
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ENALAPRILAT
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20090915
Marketing Category Name ANDA
Labeler Name Hospira, Inc.
Substance Name ENALAPRILAT
Strength Number 1.25
Strength Unit mg/mL
Pharmaceutical Classes

Complete Information of Enalaprilat


General Information