Package 68788-8510-6

{"route": ["ORAL"], "spl_id": "55b99e30-0b39-4e66-941c-fcd32fda827c", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH", "3ST302B24A"], "rxcui": ["979468"], "spl_set_id": ["0f0c7234-b605-440f-abed-44f992d189a2"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68788-8510-1)", "package_ndc": "68788-8510-1", "marketing_start_date": "20230822"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-8510-3)", "package_ndc": "68788-8510-3", "marketing_start_date": "20230822"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68788-8510-6)", "package_ndc": "68788-8510-6", "marketing_start_date": "20230822"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-8510-9)", "package_ndc": "68788-8510-9", "marketing_start_date": "20230822"}], "brand_name": "Losartan Potassium and Hydrochlorothiazide", "product_id": "68788-8510_55b99e30-0b39-4e66-941c-fcd32fda827c", "dosage_form": "TABLET", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]", "Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "68788-8510", "generic_name": "Losartan Potassium and Hydrochlorothiazide", "labeler_name": "Preferred Pharmaceuticals, Inc.", "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": "ANDA078245", "marketing_category": "ANDA", "marketing_start_date": "20230822", "listing_expiration_date": "20261231"}