Home > National Drug Code (NDC) > ENALAPRIL MALEATE

ENALAPRIL MALEATE - 24236-608-20 - (ENALAPRIL MALEATE)

Alphabetical Index


Drug Information of ENALAPRIL MALEATE

Product NDC: 24236-608
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: 24236-608
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075483
Marketing Category: ANDA
Start Marketing Date: 20130315

Package Information of ENALAPRIL MALEATE

Package NDC: 24236-608-20
Package Description: 100 TABLET in 1 CANISTER (24236-608-20)

NDC Information of ENALAPRIL MALEATE

NDC Code 24236-608-20
Proprietary Name ENALAPRIL MALEATE
Package Description 100 TABLET in 1 CANISTER (24236-608-20)
Product NDC 24236-608
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ENALAPRIL MALEATE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130315
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