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Quinapril Hydrochloride/Hydrochlorothiazide - 65862-162-30 - (Quinapril Hydrochloride/Hydrochlorothiazide)

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Drug Information of Quinapril Hydrochloride/Hydrochlorothiazide

Product NDC: 65862-162
Proprietary Name: Quinapril Hydrochloride/Hydrochlorothiazide
Non Proprietary Name: Quinapril Hydrochloride/Hydrochlorothiazide
Active Ingredient(s): 12.5; 20    mg/1; mg/1 & nbsp;   Quinapril Hydrochloride/Hydrochlorothiazide
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Quinapril Hydrochloride/Hydrochlorothiazide

Product NDC: 65862-162
Labeler Name: Aurobindo Pharma Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078450
Marketing Category: ANDA
Start Marketing Date: 20070824

Package Information of Quinapril Hydrochloride/Hydrochlorothiazide

Package NDC: 65862-162-30
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (65862-162-30)

NDC Information of Quinapril Hydrochloride/Hydrochlorothiazide

NDC Code 65862-162-30
Proprietary Name Quinapril Hydrochloride/Hydrochlorothiazide
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (65862-162-30)
Product NDC 65862-162
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Quinapril Hydrochloride/Hydrochlorothiazide
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20070824
Marketing Category Name ANDA
Labeler Name Aurobindo Pharma Limited
Substance Name HYDROCHLOROTHIAZIDE; QUINAPRIL HYDROCHLORIDE
Strength Number 12.5; 20
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 Quinapril Hydrochloride/Hydrochlorothiazide


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