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ENALAPRIL MALEATE - 67046-160-30 - (ENALAPRIL MALEATE)

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Drug Information of ENALAPRIL MALEATE

Product NDC: 67046-160
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: 67046-160
Labeler Name: Contract Pharmacy Services-PA
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075483
Marketing Category: ANDA
Start Marketing Date: 20100802

Package Information of ENALAPRIL MALEATE

Package NDC: 67046-160-30
Package Description: 30 TABLET in 1 BLISTER PACK (67046-160-30)

NDC Information of ENALAPRIL MALEATE

NDC Code 67046-160-30
Proprietary Name ENALAPRIL MALEATE
Package Description 30 TABLET in 1 BLISTER PACK (67046-160-30)
Product NDC 67046-160
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ENALAPRIL MALEATE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100802
Marketing Category Name ANDA
Labeler Name Contract Pharmacy Services-PA
Substance Name ENALAPRIL MALEATE
Strength Number 10
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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