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Quinapril Hydrochloride and Hydrochlorothiazide - 0378-0543-93 - (quinapril hydrochloride and hydrochlorothiazide)

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Drug Information of Quinapril Hydrochloride and Hydrochlorothiazide

Product NDC: 0378-0543
Proprietary Name: Quinapril Hydrochloride and Hydrochlorothiazide
Non Proprietary Name: quinapril hydrochloride and hydrochlorothiazide
Active Ingredient(s): 12.5; 20    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 Quinapril Hydrochloride and Hydrochlorothiazide

Product NDC: 0378-0543
Labeler Name: Mylan Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077093
Marketing Category: ANDA
Start Marketing Date: 20121018

Package Information of Quinapril Hydrochloride and Hydrochlorothiazide

Package NDC: 0378-0543-93
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-0543-93)

NDC Information of Quinapril Hydrochloride and Hydrochlorothiazide

NDC Code 0378-0543-93
Proprietary Name Quinapril Hydrochloride and Hydrochlorothiazide
Package Description 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-0543-93)
Product NDC 0378-0543
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 20121018
Marketing Category Name ANDA
Labeler Name Mylan Pharmaceuticals Inc.
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 and Hydrochlorothiazide


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