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ENALAPRIL MALEATE - 55154-1339-0 - (ENALAPRIL MALEATE)

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Drug Information of ENALAPRIL MALEATE

Product NDC: 55154-1339
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: 55154-1339
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075483
Marketing Category: ANDA
Start Marketing Date: 20040203

Package Information of ENALAPRIL MALEATE

Package NDC: 55154-1339-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-1339-0) > 1 TABLET in 1 BLISTER PACK

NDC Information of ENALAPRIL MALEATE

NDC Code 55154-1339-0
Proprietary Name ENALAPRIL MALEATE
Package Description 10 BLISTER PACK in 1 BAG (55154-1339-0) > 1 TABLET in 1 BLISTER PACK
Product NDC 55154-1339
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ENALAPRIL MALEATE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20040203
Marketing Category Name ANDA
Labeler Name Cardinal Health
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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