Package 50090-4447-1

{"route": ["ORAL"], "spl_id": "e0142ce8-40f3-4dd4-b37f-15859a669a62", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH", "3ST302B24A"], "rxcui": ["979471"], "spl_set_id": ["5ec290f4-bf21-4c5b-a576-8eb2bd6bd379"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-4447-0)", "package_ndc": "50090-4447-0", "marketing_start_date": "20240904"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-4447-1)", "package_ndc": "50090-4447-1", "marketing_start_date": "20240904"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (50090-4447-2)", "package_ndc": "50090-4447-2", "marketing_start_date": "20260211"}], "brand_name": "Losartan Potassium and Hydrochlorothiazide", "product_id": "50090-4447_e0142ce8-40f3-4dd4-b37f-15859a669a62", "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": "50090-4447", "generic_name": "Losartan Potassium and Hydrochlorothiazide", "labeler_name": "A-S Medication Solutions", "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": "20240904", "listing_expiration_date": "20271231"}