Package 68788-8187-1

{"route": ["ORAL"], "spl_id": "89e06172-44a8-4129-bda1-06c7505c9728", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH", "3ST302B24A"], "rxcui": ["979468"], "spl_set_id": ["46cf633d-70a5-4d3b-b349-ad74c23ddace"], "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, FILM COATED in 1 BOTTLE (68788-8187-1)", "package_ndc": "68788-8187-1", "marketing_start_date": "20220510"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68788-8187-3)", "package_ndc": "68788-8187-3", "marketing_start_date": "20220510"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68788-8187-6)", "package_ndc": "68788-8187-6", "marketing_start_date": "20220510"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68788-8187-9)", "package_ndc": "68788-8187-9", "marketing_start_date": "20220510"}], "brand_name": "Losartan Potassium and Hydrochlorothiazide", "product_id": "68788-8187_89e06172-44a8-4129-bda1-06c7505c9728", "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": "68788-8187", "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": "ANDA204901", "marketing_category": "ANDA", "marketing_start_date": "20220510", "listing_expiration_date": "20261231"}