Package 72162-2328-1

{"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"}