Quinapril - 63629-1241-2 - (Quinapril)

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Drug Information of Quinapril

Product NDC: 63629-1241
Proprietary Name: Quinapril
Non Proprietary Name: Quinapril
Active Ingredient(s): 20    mg/1 & nbsp;   Quinapril
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Quinapril

Product NDC: 63629-1241
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075504
Marketing Category: ANDA
Start Marketing Date: 20100225

Package Information of Quinapril

Package NDC: 63629-1241-2
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE (63629-1241-2)

NDC Information of Quinapril

NDC Code 63629-1241-2
Proprietary Name Quinapril
Package Description 90 TABLET, FILM COATED in 1 BOTTLE (63629-1241-2)
Product NDC 63629-1241
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Quinapril
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20100225
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name QUINAPRIL HYDROCHLORIDE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]

Complete Information of Quinapril


General Information