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Enalapril Maleate - 0093-0028-50 - (Enalapril Maleate)

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Drug Information of Enalapril Maleate

Product NDC: 0093-0028
Proprietary Name: Enalapril Maleate
Non Proprietary Name: Enalapril Maleate
Active Ingredient(s): 10    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: 0093-0028
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075479
Marketing Category: ANDA
Start Marketing Date: 20000823

Package Information of Enalapril Maleate

Package NDC: 0093-0028-50
Package Description: 5000 TABLET in 1 BOTTLE (0093-0028-50)

NDC Information of Enalapril Maleate

NDC Code 0093-0028-50
Proprietary Name Enalapril Maleate
Package Description 5000 TABLET in 1 BOTTLE (0093-0028-50)
Product NDC 0093-0028
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Enalapril Maleate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20000823
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
Substance Name ENALAPRIL MALEATE
Strength Number 10
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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