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Enalaprilat - 55154-0355-5 - (Enalaprilat)

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Drug Information of Enalaprilat

Product NDC: 55154-0355
Proprietary Name: Enalaprilat
Non Proprietary Name: Enalaprilat
Active Ingredient(s): 1.25    mg/mL & nbsp;   Enalaprilat
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Enalaprilat

Product NDC: 55154-0355
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075634
Marketing Category: ANDA
Start Marketing Date: 20000823

Package Information of Enalaprilat

Package NDC: 55154-0355-5
Package Description: 5 VIAL in 1 BAG (55154-0355-5) > 1 mL in 1 VIAL

NDC Information of Enalaprilat

NDC Code 55154-0355-5
Proprietary Name Enalaprilat
Package Description 5 VIAL in 1 BAG (55154-0355-5) > 1 mL in 1 VIAL
Product NDC 55154-0355
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Enalaprilat
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 20000823
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name ENALAPRILAT
Strength Number 1.25
Strength Unit mg/mL
Pharmaceutical Classes Angiontensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE]

Complete Information of Enalaprilat


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