Home > National Drug Code (NDC) > Quinapril Hydrochloride and Hydrochlorothiazide

Quinapril Hydrochloride and Hydrochlorothiazide - 31722-376-90 - (Quinapril Hydrochloride and Hydrochlorothiazide)

Alphabetical Index


Drug Information of Quinapril Hydrochloride and Hydrochlorothiazide

Product NDC: 31722-376
Proprietary Name: Quinapril Hydrochloride and Hydrochlorothiazide
Non Proprietary Name: Quinapril Hydrochloride and Hydrochlorothiazide
Active Ingredient(s): 25; 20    mg/1; mg/1 & nbsp;   Quinapril Hydrochloride and Hydrochlorothiazide
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Quinapril Hydrochloride and Hydrochlorothiazide

Product NDC: 31722-376
Labeler Name: Camber Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA201356
Marketing Category: ANDA
Start Marketing Date: 20111215

Package Information of Quinapril Hydrochloride and Hydrochlorothiazide

Package NDC: 31722-376-90
Package Description: 90 TABLET in 1 BOTTLE (31722-376-90)

NDC Information of Quinapril Hydrochloride and Hydrochlorothiazide

NDC Code 31722-376-90
Proprietary Name Quinapril Hydrochloride and Hydrochlorothiazide
Package Description 90 TABLET in 1 BOTTLE (31722-376-90)
Product NDC 31722-376
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Quinapril Hydrochloride and Hydrochlorothiazide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20111215
Marketing Category Name ANDA
Labeler Name Camber Pharmaceuticals
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 Hydrochloride and Hydrochlorothiazide


General Information