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Enalapril Maleate - 51138-036-30 - (Enalapril Maleate)

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Drug Information of Enalapril Maleate

Product NDC: 51138-036
Proprietary Name: Enalapril Maleate
Non Proprietary Name: Enalapril Maleate
Active Ingredient(s): 20    mg/1 & nbsp;   Enalapril Maleate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Enalapril Maleate

Product NDC: 51138-036
Labeler Name: Med Health Pharma, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075483
Marketing Category: ANDA
Start Marketing Date: 20110101

Package Information of Enalapril Maleate

Package NDC: 51138-036-30
Package Description: 30 TABLET in 1 BOTTLE (51138-036-30)

NDC Information of Enalapril Maleate

NDC Code 51138-036-30
Proprietary Name Enalapril Maleate
Package Description 30 TABLET in 1 BOTTLE (51138-036-30)
Product NDC 51138-036
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Enalapril Maleate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110101
Marketing Category Name ANDA
Labeler Name Med Health Pharma, LLC
Substance Name ENALAPRIL MALEATE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE]

Complete Information of Enalapril Maleate


General Information