quinapril and hydrochlorothiazide (62135-669)

Drug Facts

Product Profile

Brand Name quinapril and hydrochlorothiazide

Generic Name quinapril and hydrochlorothiazide

Labeler chartwell rx, llc

Dosage Form TABLET

Routes

ORAL

Active Ingredients

hydrochlorothiazide 25 mg/1, quinapril hydrochloride 20 mg/1

Manufacturer

Chartwell RX, LLC

Identifiers & Regulatory

Product NDC 62135-669

Product ID 62135-669_0c3f4504-d57e-aa79-e063-6294a90ad5b8

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA076374

Listing Expiration 2026-12-31

Marketing Start 2004-03-31

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 62135669

Hyphenated Format 62135-669

Supplemental Identifiers

RxCUI

310796 310797 310809

UPC

0362135669904 0362135667900 0362135668907

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 and hydrochlorothiazide (source: ndc)

Generic Name quinapril and hydrochlorothiazide (source: ndc)

Application Number ANDA076374 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

25 mg/1
20 mg/1

source: ndc

Packaging

90 TABLET in 1 BOTTLE (62135-669-90)

source: ndc

Packages (1)

62135-669-90 90 TABLET in 1 BOTTLE (62135-669-90)

Ingredients (2)

hydrochlorothiazide (25 mg/1) quinapril hydrochloride (20 mg/1)

Linked Drug Pages (1)

Quinapril and Hydrochlorothiazide ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["ORAL"], "spl_id": "0c3f4504-d57e-aa79-e063-6294a90ad5b8", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0362135669904", "0362135667900", "0362135668907"], "unii": ["0J48LPH2TH", "33067B3N2M"], "rxcui": ["310796", "310797", "310809"], "spl_set_id": ["2eae533f-d0af-47e8-a1f2-94bc8cc89b5a"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (62135-669-90)", "package_ndc": "62135-669-90", "marketing_start_date": "20231205"}], "brand_name": "Quinapril and Hydrochlorothiazide", "product_id": "62135-669_0c3f4504-d57e-aa79-e063-6294a90ad5b8", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "62135-669", "generic_name": "Quinapril and Hydrochlorothiazide", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Quinapril and Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "25 mg/1"}, {"name": "QUINAPRIL HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA076374", "marketing_category": "ANDA", "marketing_start_date": "20040331", "listing_expiration_date": "20261231"}