Quinapril - 42291-701-90 - (Quinapril)

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Drug Information of Quinapril

Product NDC: 42291-701
Proprietary Name: Quinapril
Non Proprietary Name: Quinapril
Active Ingredient(s): 5    mg/1 & nbsp;   Quinapril
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Quinapril

Product NDC: 42291-701
Labeler Name: AvKARE, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078457
Marketing Category: ANDA
Start Marketing Date: 20120802

Package Information of Quinapril

Package NDC: 42291-701-90
Package Description: 90 TABLET in 1 BOTTLE (42291-701-90)

NDC Information of Quinapril

NDC Code 42291-701-90
Proprietary Name Quinapril
Package Description 90 TABLET in 1 BOTTLE (42291-701-90)
Product NDC 42291-701
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Quinapril
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120802
Marketing Category Name ANDA
Labeler Name AvKARE, Inc.
Substance Name QUINAPRIL HYDROCHLORIDE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]

Complete Information of Quinapril


General Information