benazepril hydrochloride and hydrochlorothiazide

Generic: benazepril hydrochloride and hydrochlorothiazide

Labeler: advagen pharma ltd
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 advagen pharma ltd
Dosage Form TABLET
Routes
ORAL
Active Ingredients

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

Manufacturer
Advagen Pharma Ltd

Identifiers & Regulatory

Product NDC 72888-220
Product ID 72888-220_4b924079-c490-67c8-e063-6394a90aa7d0
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA AUTHORIZED GENERIC
Application Number NDA020033
Listing Expiration 2027-12-31
Marketing Start 2024-12-05

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 72888220
Hyphenated Format 72888-220

Supplemental Identifiers

RxCUI
898362 898367 898372
UPC
0372888220017 0372888222011
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 NDA020033 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
  • 12.5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (72888-220-01)
source: ndc

Packages (1)

72888-220-01 100 TABLET in 1 BOTTLE (72888-220-01)

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": "4b924079-c490-67c8-e063-6394a90aa7d0", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0372888220017", "0372888222011"], "unii": ["0J48LPH2TH", "N1SN99T69T"], "rxcui": ["898362", "898367", "898372"], "spl_set_id": ["3f6e6da8-6da3-47c5-a151-e6fd7206890e"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Advagen Pharma Ltd"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72888-220-01)", "package_ndc": "72888-220-01", "marketing_start_date": "20241205"}], "brand_name": "benazepril hydrochloride and hydrochlorothiazide", "product_id": "72888-220_4b924079-c490-67c8-e063-6394a90aa7d0", "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": "72888-220", "generic_name": "benazepril hydrochloride and hydrochlorothiazide", "labeler_name": "Advagen Pharma Ltd", "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": "NDA020033", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20241205", "listing_expiration_date": "20271231"}