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Enalapril Maleate - 60505-0052-9 - (enalapril maleate)

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Drug Information of Enalapril Maleate

Product NDC: 60505-0052
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: 60505-0052
Labeler Name: Apotex Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075178
Marketing Category: ANDA
Start Marketing Date: 20010323

Package Information of Enalapril Maleate

Package NDC: 60505-0052-9
Package Description: 1000 TABLET in 1 BOTTLE (60505-0052-9)

NDC Information of Enalapril Maleate

NDC Code 60505-0052-9
Proprietary Name Enalapril Maleate
Package Description 1000 TABLET in 1 BOTTLE (60505-0052-9)
Product NDC 60505-0052
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name enalapril maleate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20010323
Marketing Category Name ANDA
Labeler Name Apotex Corp.
Substance Name ENALAPRIL MALEATE
Strength Number 20
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


General Information