Package 72189-288-90

{"route": ["ORAL"], "spl_id": "2c2941f2-b8cb-a99a-e063-6294a90ab626", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH", "3ST302B24A"], "rxcui": ["979471"], "spl_set_id": ["cf4278a3-fbb7-a8ab-e053-2a95a90abc0f"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["DirectRx"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (72189-288-90)", "package_ndc": "72189-288-90", "marketing_start_date": "20211026"}], "brand_name": "LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE", "product_id": "72189-288_2c2941f2-b8cb-a99a-e063-6294a90ab626", "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": "72189-288", "generic_name": "LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE", "labeler_name": "DirectRx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "25 mg/1"}, {"name": "LOSARTAN POTASSIUM", "strength": "100 mg/1"}], "application_number": "ANDA091629", "marketing_category": "ANDA", "marketing_start_date": "20211026", "listing_expiration_date": "20261231"}