Quinapril - 68180-558-03 - (Quinapril)

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Drug Information of Quinapril

Product NDC: 68180-558
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: 68180-558
Labeler Name: Lupin Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077690
Marketing Category: ANDA
Start Marketing Date: 20070226

Package Information of Quinapril

Package NDC: 68180-558-03
Package Description: 1000 TABLET in 1 BOTTLE (68180-558-03)

NDC Information of Quinapril

NDC Code 68180-558-03
Proprietary Name Quinapril
Package Description 1000 TABLET in 1 BOTTLE (68180-558-03)
Product NDC 68180-558
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Quinapril
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070226
Marketing Category Name ANDA
Labeler Name Lupin Pharmaceuticals, 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