Package 16714-226-01

{"route": ["ORAL"], "spl_id": "d3aeeeca-2c3a-4006-89f7-e3836aa8399b", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH", "3ST302B24A"], "rxcui": ["979464", "979468", "979471"], "spl_set_id": ["25318baf-9c2f-458f-b9ea-f52dabca49af"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["NorthStar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (16714-226-01)", "package_ndc": "16714-226-01", "marketing_start_date": "20240904"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (16714-226-02)", "package_ndc": "16714-226-02", "marketing_start_date": "20240904"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (16714-226-04)", "package_ndc": "16714-226-04", "marketing_start_date": "20240904"}], "brand_name": "Losartan Potassium and Hydrochlorothiazide", "product_id": "16714-226_d3aeeeca-2c3a-4006-89f7-e3836aa8399b", "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": "16714-226", "generic_name": "Losartan Potassium and Hydrochlorothiazide", "labeler_name": "NorthStar Rx LLC", "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": "ANDA091629", "marketing_category": "ANDA", "marketing_start_date": "20240904", "listing_expiration_date": "20261231"}