Accupril - 0071-0532-23 - (QUINAPRIL HYDROCHLORIDE)

Alphabetical Index


Drug Information of Accupril

Product NDC: 0071-0532
Proprietary Name: Accupril
Non Proprietary Name: QUINAPRIL HYDROCHLORIDE
Active Ingredient(s): 20    mg/1 & nbsp;   QUINAPRIL HYDROCHLORIDE
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Accupril

Product NDC: 0071-0532
Labeler Name: Parke-Davis Div of Pfizer Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019885
Marketing Category: NDA
Start Marketing Date: 19911119

Package Information of Accupril

Package NDC: 0071-0532-23
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE (0071-0532-23)

NDC Information of Accupril

NDC Code 0071-0532-23
Proprietary Name Accupril
Package Description 90 TABLET, FILM COATED in 1 BOTTLE (0071-0532-23)
Product NDC 0071-0532
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name QUINAPRIL HYDROCHLORIDE
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19911119
Marketing Category Name NDA
Labeler Name Parke-Davis Div of Pfizer 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 Accupril


General Information