Package 72888-220-01

Brand: benazepril hydrochloride and hydrochlorothiazide

Generic: benazepril hydrochloride and hydrochlorothiazide
NDC Package

Package Facts

Identity

Package NDC 72888-220-01
Digits Only 7288822001
Product NDC 72888-220
Description

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

Marketing

Marketing Status
Marketed Since 2024-12-05
Brand benazepril hydrochloride and hydrochlorothiazide
Generic benazepril hydrochloride and hydrochlorothiazide
Sample Package No

Linked Drug Pages (1)

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"}