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Enalapril Maleate - 52125-426-02 - (Enalapril Maleate)

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Drug Information of Enalapril Maleate

Product NDC: 52125-426
Proprietary Name: Enalapril Maleate
Non Proprietary Name: Enalapril Maleate
Active Ingredient(s): 20    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: 52125-426
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075479
Marketing Category: ANDA
Start Marketing Date: 20130515

Package Information of Enalapril Maleate

Package NDC: 52125-426-02
Package Description: 30 TABLET in 1 BLISTER PACK (52125-426-02)

NDC Information of Enalapril Maleate

NDC Code 52125-426-02
Proprietary Name Enalapril Maleate
Package Description 30 TABLET in 1 BLISTER PACK (52125-426-02)
Product NDC 52125-426
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Enalapril Maleate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130515
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name ENALAPRIL MALEATE
Strength Number 20
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


General Information