benazepril hydrochloride and hydrochlorothiazide (0185-0325)

Drug Facts

Product Profile

Brand Name benazepril hydrochloride and hydrochlorothiazide

Generic Name benazepril hydrochloride and hydrochlorothiazide

Labeler sandoz inc

Dosage Form TABLET, FILM COATED

Routes

ORAL

Active Ingredients

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

Manufacturer

Sandoz Inc

Identifiers & Regulatory

Product NDC 0185-0325

Product ID 0185-0325_d9ded9f8-b60e-4325-a813-44b5ee485acc

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA076631

Listing Expiration 2026-12-31

Marketing Start 2014-04-04

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 01850325

Hyphenated Format 0185-0325

Supplemental Identifiers

RxCUI

898362 898367 898372 898378

UPC

0301850325016 0301850236015 0301850277018 0301850211012

UNII

0J48LPH2TH N1SN99T69T

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 benazepril hydrochloride and hydrochlorothiazide (source: ndc)

Generic Name benazepril hydrochloride and hydrochlorothiazide (source: ndc)

Application Number ANDA076631 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

10 mg/1
12.5 mg/1

source: ndc

Packaging

100 TABLET, FILM COATED in 1 BOTTLE (0185-0325-01)

source: ndc

Packages (1)

0185-0325-01 100 TABLET, FILM COATED in 1 BOTTLE (0185-0325-01)

Ingredients (2)

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

Linked Drug Pages (1)

Benazepril Hydrochloride and Hydrochlorothiazide ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["ORAL"], "spl_id": "d9ded9f8-b60e-4325-a813-44b5ee485acc", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0301850325016", "0301850236015", "0301850277018", "0301850211012"], "unii": ["0J48LPH2TH", "N1SN99T69T"], "rxcui": ["898362", "898367", "898372", "898378"], "spl_set_id": ["c9bdfbb4-87b6-4de4-bc1d-5025d3ef591f"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (0185-0325-01)", "package_ndc": "0185-0325-01", "marketing_start_date": "20140404"}], "brand_name": "Benazepril Hydrochloride and Hydrochlorothiazide", "product_id": "0185-0325_d9ded9f8-b60e-4325-a813-44b5ee485acc", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]", "Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "0185-0325", "generic_name": "Benazepril Hydrochloride and Hydrochlorothiazide", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Benazepril Hydrochloride and Hydrochlorothiazide", "active_ingredients": [{"name": "BENAZEPRIL HYDROCHLORIDE", "strength": "10 mg/1"}, {"name": "HYDROCHLOROTHIAZIDE", "strength": "12.5 mg/1"}], "application_number": "ANDA076631", "marketing_category": "ANDA", "marketing_start_date": "20140404", "listing_expiration_date": "20261231"}