Package 72162-2461-0

{"route": ["ORAL"], "spl_id": "1c647f86-de31-4e1b-84c2-5a3d15bc1c70", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH", "3ST302B24A"], "rxcui": ["979464"], "spl_set_id": ["f9cfb39e-4367-40a0-86ee-138645aace56"], "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": "1000 TABLET, FILM COATED in 1 BOTTLE (72162-2461-0)", "package_ndc": "72162-2461-0", "marketing_start_date": "20250221"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72162-2461-3)", "package_ndc": "72162-2461-3", "marketing_start_date": "20250221"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (72162-2461-9)", "package_ndc": "72162-2461-9", "marketing_start_date": "20250221"}], "brand_name": "losartan potassium and hydrochlorothiazide", "product_id": "72162-2461_1c647f86-de31-4e1b-84c2-5a3d15bc1c70", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]", "Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "72162-2461", "generic_name": "losartan potassium and hydrochlorothiazide", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "losartan potassium and hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "12.5 mg/1"}, {"name": "LOSARTAN POTASSIUM", "strength": "100 mg/1"}], "application_number": "ANDA204832", "marketing_category": "ANDA", "marketing_start_date": "20170721", "listing_expiration_date": "20261231"}