Quinapril - 54868-5241-0 - (quinapril)

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Drug Information of Quinapril

Product NDC: 54868-5241
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: 54868-5241
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076607
Marketing Category: ANDA
Start Marketing Date: 20050303

Package Information of Quinapril

Package NDC: 54868-5241-0
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (54868-5241-0)

NDC Information of Quinapril

NDC Code 54868-5241-0
Proprietary Name Quinapril
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (54868-5241-0)
Product NDC 54868-5241
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name quinapril
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20050303
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
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