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Quinapril HCl and Hydrochlorothiazide - 43386-712-09 - (Quinapril HCl and Hydrochlorothiazide)

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Drug Information of Quinapril HCl and Hydrochlorothiazide

Product NDC: 43386-712
Proprietary Name: Quinapril HCl and Hydrochlorothiazide
Non Proprietary Name: Quinapril HCl and Hydrochlorothiazide
Active Ingredient(s): 25; 20    mg/1; mg/1 & nbsp;   Quinapril HCl and Hydrochlorothiazide
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Quinapril HCl and Hydrochlorothiazide

Product NDC: 43386-712
Labeler Name: GAVIS Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076374
Marketing Category: ANDA
Start Marketing Date: 20110715

Package Information of Quinapril HCl and Hydrochlorothiazide

Package NDC: 43386-712-09
Package Description: 90 TABLET in 1 BOTTLE (43386-712-09)

NDC Information of Quinapril HCl and Hydrochlorothiazide

NDC Code 43386-712-09
Proprietary Name Quinapril HCl and Hydrochlorothiazide
Package Description 90 TABLET in 1 BOTTLE (43386-712-09)
Product NDC 43386-712
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Quinapril HCl and Hydrochlorothiazide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110715
Marketing Category Name ANDA
Labeler Name GAVIS Pharmaceuticals, LLC
Substance Name HYDROCHLOROTHIAZIDE; QUINAPRIL HYDROCHLORIDE
Strength Number 25; 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 HCl and Hydrochlorothiazide


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