Package 71335-2572-3

{"route": ["ORAL"], "spl_id": "367a96b9-9983-4c67-acea-7ab1f44ea7f3", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH", "3ST302B24A"], "rxcui": ["979464"], "spl_set_id": ["e0f63126-6890-48bf-9c25-444dc5974ecd"], "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": "30 TABLET, FILM COATED in 1 BOTTLE (71335-2572-1)", "package_ndc": "71335-2572-1", "marketing_start_date": "20250205"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-2572-2)", "package_ndc": "71335-2572-2", "marketing_start_date": "20250205"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (71335-2572-3)", "package_ndc": "71335-2572-3", "marketing_start_date": "20250205"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (71335-2572-4)", "package_ndc": "71335-2572-4", "marketing_start_date": "20250205"}], "brand_name": "Losartan Potassium and Hydrochlorothiazide", "product_id": "71335-2572_367a96b9-9983-4c67-acea-7ab1f44ea7f3", "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": "71335-2572", "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": "ANDA204901", "marketing_category": "ANDA", "marketing_start_date": "20180215", "listing_expiration_date": "20261231"}