benazepril hydrochloride and hydrochlorothiazide (0185-0236)

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 5 mg/1, hydrochlorothiazide 6.25 mg/1

Manufacturer

Sandoz Inc

Identifiers & Regulatory

Product NDC 0185-0236

Product ID 0185-0236_d9ded9f8-b60e-4325-a813-44b5ee485acc

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA076631

Listing Expiration 2026-12-31

Marketing Start 2015-03-17

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 01850236

Hyphenated Format 0185-0236

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

5 mg/1
6.25 mg/1

source: ndc

Packaging

100 TABLET, FILM COATED in 1 BOTTLE (0185-0236-01)

source: ndc

Packages (1)

0185-0236-01 100 TABLET, FILM COATED in 1 BOTTLE (0185-0236-01)

Ingredients (2)

benazepril hydrochloride (5 mg/1) hydrochlorothiazide (6.25 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 (0185-0236-01)", "package_ndc": "0185-0236-01", "marketing_start_date": "20150317"}], "brand_name": "Benazepril Hydrochloride and Hydrochlorothiazide", "product_id": "0185-0236_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": "0185-0236", "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": "5 mg/1"}, {"name": "HYDROCHLOROTHIAZIDE", "strength": "6.25 mg/1"}], "application_number": "ANDA076631", "marketing_category": "ANDA", "marketing_start_date": "20150317", "listing_expiration_date": "20261231"}