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ENALAPRIL MALEATE - 50436-6859-1 - (ENALAPRIL MALEATE)

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Drug Information of ENALAPRIL MALEATE

Product NDC: 50436-6859
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: 50436-6859
Labeler Name: Unit Dose Services
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075483
Marketing Category: ANDA
Start Marketing Date: 20091211

Package Information of ENALAPRIL MALEATE

Package NDC: 50436-6859-1
Package Description: 30 TABLET in 1 BOTTLE (50436-6859-1)

NDC Information of ENALAPRIL MALEATE

NDC Code 50436-6859-1
Proprietary Name ENALAPRIL MALEATE
Package Description 30 TABLET in 1 BOTTLE (50436-6859-1)
Product NDC 50436-6859
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ENALAPRIL MALEATE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20091211
Marketing Category Name ANDA
Labeler Name Unit Dose Services
Substance Name ENALAPRIL MALEATE
Strength Number 5
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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