benazepril hydrochloride and hydrochlorothiazide

Generic: benazepril hydrochloride and hydrochlorothiazide

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG NDA AUTHORIZED GENERIC Inactive Finished

Drug Facts

Product Profile

Brand Name benazepril hydrochloride and hydrochlorothiazide
Generic Name benazepril hydrochloride and hydrochlorothiazide
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

benazepril hydrochloride 20 mg/1, hydrochlorothiazide 12.5 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 72162-2328
Product ID 72162-2328_8c875109-8488-4162-9a8c-d679347c4c0a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA AUTHORIZED GENERIC
Application Number NDA020033
Listing Expiration 2026-12-31
Marketing Start 2019-04-07

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 721622328
Hyphenated Format 72162-2328

Supplemental Identifiers

RxCUI
898367
UNII
N1SN99T69T 0J48LPH2TH
NUI
N0000175359 N0000175419 M0471776

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 NDA020033 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
  • 12.5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (72162-2328-1)
source: ndc

Packages (1)

72162-2328-1 100 TABLET in 1 BOTTLE (72162-2328-1)

Ingredients (2)

benazepril hydrochloride (20 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": "8c875109-8488-4162-9a8c-d679347c4c0a", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["N1SN99T69T", "0J48LPH2TH"], "rxcui": ["898367"], "spl_set_id": ["f4120568-dd9b-47a5-bd44-4de6ed343bbe"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-2328-1)", "package_ndc": "72162-2328-1", "marketing_start_date": "20240618"}], "brand_name": "benazepril hydrochloride and hydrochlorothiazide", "product_id": "72162-2328_8c875109-8488-4162-9a8c-d679347c4c0a", "dosage_form": "TABLET", "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": "72162-2328", "generic_name": "benazepril hydrochloride and hydrochlorothiazide", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "benazepril hydrochloride and hydrochlorothiazide", "active_ingredients": [{"name": "BENAZEPRIL HYDROCHLORIDE", "strength": "20 mg/1"}, {"name": "HYDROCHLOROTHIAZIDE", "strength": "12.5 mg/1"}], "application_number": "NDA020033", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20190407", "listing_expiration_date": "20261231"}