quinapril hydrochloride/hydrochlorothiazide (65862-161)

Drug Facts

Product Profile

Brand Name quinapril hydrochloride/hydrochlorothiazide

Generic Name quinapril hydrochloride/hydrochlorothiazide

Labeler aurobindo pharma limited

Dosage Form TABLET, FILM COATED

Routes

ORAL

Active Ingredients

hydrochlorothiazide 12.5 mg/1, quinapril hydrochloride 10 mg/1

Manufacturer

Aurobindo Pharma Limited

Identifiers & Regulatory

Product NDC 65862-161

Product ID 65862-161_5842ecc2-874a-481b-8997-afa9d862dc5d

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA078450

Listing Expiration 2026-12-31

Marketing Start 2007-08-24

Pharmacologic Class

Established (EPC)

thiazide diuretic [epc]

Chemical Structure

thiazides [cs]

Physiologic Effect

increased diuresis [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 65862161

Hyphenated Format 65862-161

Supplemental Identifiers

RxCUI

310796 310797 310809

UPC

0365862161901

UNII

0J48LPH2TH 33067B3N2M

NUI

N0000175359 N0000175419 M0471776

Packaging Origin

Original Packager

true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name quinapril hydrochloride/hydrochlorothiazide (source: ndc)

Generic Name quinapril hydrochloride/hydrochlorothiazide (source: ndc)

Application Number ANDA078450 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

12.5 mg/1
10 mg/1

source: ndc

Packaging

90 TABLET, FILM COATED in 1 BOTTLE (65862-161-90)

source: ndc

Packages (1)

65862-161-90 90 TABLET, FILM COATED in 1 BOTTLE (65862-161-90)

Ingredients (2)

hydrochlorothiazide (12.5 mg/1) quinapril hydrochloride (10 mg/1)

Linked Drug Pages (1)

QUINAPRIL HYDROCHLORIDE/HYDROCHLOROTHIAZIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

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