Package 72189-129-90

{"route": ["ORAL"], "spl_id": "2becfaea-c7d6-ec34-e063-6294a90af5b3", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH", "3ST302B24A"], "rxcui": ["979464", "979468", "979471"], "spl_set_id": ["8de04bf2-83dd-c494-e053-2a95a90abade"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72189-129-30)", "package_ndc": "72189-129-30", "marketing_start_date": "20201015"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (72189-129-90)", "package_ndc": "72189-129-90", "marketing_start_date": "20201015"}], "brand_name": "LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE", "product_id": "72189-129_2becfaea-c7d6-ec34-e063-6294a90af5b3", "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": "72189-129", "generic_name": "losartan potassium and hydrochlorothiazide", "labeler_name": "Direct_Rx", "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": "50 mg/1"}], "application_number": "ANDA201845", "marketing_category": "ANDA", "marketing_start_date": "20201015", "listing_expiration_date": "20261231"}