ACCURETIC - 0071-0222-23 - (QUINAPRIL HYDROCHLORIDE and HYDROCHLOROTHIAZIDE)

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Drug Information of ACCURETIC

Product NDC: 0071-0222
Proprietary Name: ACCURETIC
Non Proprietary Name: QUINAPRIL HYDROCHLORIDE and HYDROCHLOROTHIAZIDE
Active Ingredient(s): 12.5; 10    mg/1; mg/1 & nbsp;   QUINAPRIL HYDROCHLORIDE and HYDROCHLOROTHIAZIDE
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of ACCURETIC

Product NDC: 0071-0222
Labeler Name: Parke-Davis Div of Pfizer Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020125
Marketing Category: NDA
Start Marketing Date: 19991228

Package Information of ACCURETIC

Package NDC: 0071-0222-23
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE (0071-0222-23)

NDC Information of ACCURETIC

NDC Code 0071-0222-23
Proprietary Name ACCURETIC
Package Description 90 TABLET, FILM COATED in 1 BOTTLE (0071-0222-23)
Product NDC 0071-0222
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name QUINAPRIL HYDROCHLORIDE and HYDROCHLOROTHIAZIDE
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19991228
Marketing Category Name NDA
Labeler Name Parke-Davis Div of Pfizer Inc
Substance Name HYDROCHLOROTHIAZIDE; QUINAPRIL HYDROCHLORIDE
Strength Number 12.5; 10
Strength Unit mg/1; mg/1
Pharmaceutical Classes Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient]

Complete Information of ACCURETIC


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