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ENALAPRIL MALEATE - 68084-390-01 - (ENALAPRIL MALEATE)

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Drug Information of ENALAPRIL MALEATE

Product NDC: 68084-390
Proprietary Name: ENALAPRIL MALEATE
Non Proprietary Name: ENALAPRIL MALEATE
Active Ingredient(s): 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: 68084-390
Labeler Name: American Health Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075483
Marketing Category: ANDA
Start Marketing Date: 20090526

Package Information of ENALAPRIL MALEATE

Package NDC: 68084-390-01
Package Description: 10 BLISTER PACK in 1 CARTON (68084-390-01) > 10 TABLET in 1 BLISTER PACK (68084-390-11)

NDC Information of ENALAPRIL MALEATE

NDC Code 68084-390-01
Proprietary Name ENALAPRIL MALEATE
Package Description 10 BLISTER PACK in 1 CARTON (68084-390-01) > 10 TABLET in 1 BLISTER PACK (68084-390-11)
Product NDC 68084-390
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ENALAPRIL MALEATE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090526
Marketing Category Name ANDA
Labeler Name American Health Packaging
Substance Name ENALAPRIL MALEATE
Strength Number 5
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


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