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Enalapril Maleate - 0378-1051-01 - (enalapril maleate)

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Drug Information of Enalapril Maleate

Product NDC: 0378-1051
Proprietary Name: Enalapril Maleate
Non Proprietary Name: enalapril maleate
Active Ingredient(s): 2.5    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: 0378-1051
Labeler Name: Mylan Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075480
Marketing Category: ANDA
Start Marketing Date: 20000822

Package Information of Enalapril Maleate

Package NDC: 0378-1051-01
Package Description: 100 TABLET in 1 BOTTLE, PLASTIC (0378-1051-01)

NDC Information of Enalapril Maleate

NDC Code 0378-1051-01
Proprietary Name Enalapril Maleate
Package Description 100 TABLET in 1 BOTTLE, PLASTIC (0378-1051-01)
Product NDC 0378-1051
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name enalapril maleate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20000822
Marketing Category Name ANDA
Labeler Name Mylan Pharmaceuticals Inc.
Substance Name ENALAPRIL MALEATE
Strength Number 2.5
Strength Unit mg/1
Pharmaceutical Classes Angiontensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE]

Complete Information of Enalapril Maleate


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