Quinapril Hydrochloride and Hydrochlorothiazide (Ranbaxy Pharmaceuticals Inc.)


Welcome to the PulseAid listing for the Quinapril Hydrochloride and Hydrochlorothiazide drug offered from Ranbaxy Pharmaceuticals Inc.. This Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient],Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA] pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN PRESCRIPTION DRUG drug type category.
LABELER NAME / MANUFACTURER: Ranbaxy Pharmaceuticals Inc.
NON-PROPRIETARY NAME: Quinapril Hydrochloride and Hydrochlorothiazide
SUBSTANCE NAME: HYDROCHLOROTHIAZIDE; QUINAPRIL HYDROCHLORIDE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient],Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]
ROUTE: ORAL
DOSAGE FORM: TABLET, FILM COATED
MARKETING CATEGORY NAME: ANDA
START MARKETING DATE: 2009-03-04
END MARKETING DATE: 0000-00-00


Quinapril Hydrochloride and Hydrochlorothiazide HUMAN PRESCRIPTION DRUG Details:

Item DescriptionQuinapril Hydrochloride and Hydrochlorothiazide from Ranbaxy Pharmaceuticals Inc.
LABELER NAME: Ranbaxy Pharmaceuticals Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 12.5; 10(mg/1; mg/1)
START MARKETING DATE: 2009-03-04
END MARKETING DATE: 0000-00-00
PRODUCT ID: 63304-161_91baf595-84c1-47db-89b2-e6590d282dec
PRODUCT NDC: 63304-161
APPLICATION NUMBER: ANDA078211

Other HYDROCHLOROTHIAZIDE; QUINAPRIL HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Ranbaxy Pharmaceuticals Inc.Quinapril Hydrochloride and Hydrochlorothiazide