Quinapril - 31722-269-10 - (Quinapril)

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Drug Information of Quinapril

Product NDC: 31722-269
Proprietary Name: Quinapril
Non Proprietary Name: Quinapril
Active Ingredient(s): 20    mg/1 & nbsp;   Quinapril
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Quinapril

Product NDC: 31722-269
Labeler Name: Camber Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078457
Marketing Category: ANDA
Start Marketing Date: 20120120

Package Information of Quinapril

Package NDC: 31722-269-10
Package Description: 24 BOTTLE in 1 CASE (31722-269-10) > 1000 TABLET in 1 BOTTLE

NDC Information of Quinapril

NDC Code 31722-269-10
Proprietary Name Quinapril
Package Description 24 BOTTLE in 1 CASE (31722-269-10) > 1000 TABLET in 1 BOTTLE
Product NDC 31722-269
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Quinapril
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120120
Marketing Category Name ANDA
Labeler Name Camber Pharmaceuticals
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