Package 71335-2662-2

{"route": ["ORAL"], "spl_id": "de121cef-3137-4100-9489-f7c6a50faba8", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH", "3ST302B24A"], "rxcui": ["979464"], "spl_set_id": ["eb423f4b-8104-4406-bfc2-8943e517329f"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-2662-1)", "package_ndc": "71335-2662-1", "marketing_start_date": "20250626"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-2662-2)", "package_ndc": "71335-2662-2", "marketing_start_date": "20250626"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (71335-2662-3)", "package_ndc": "71335-2662-3", "marketing_start_date": "20250626"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (71335-2662-4)", "package_ndc": "71335-2662-4", "marketing_start_date": "20250626"}], "brand_name": "losartan potassium and hydrochlorothiazide", "product_id": "71335-2662_de121cef-3137-4100-9489-f7c6a50faba8", "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": "71335-2662", "generic_name": "losartan potassium and hydrochlorothiazide", "labeler_name": "Bryant Ranch Prepack", "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": "100 mg/1"}], "application_number": "ANDA204832", "marketing_category": "ANDA", "marketing_start_date": "20170721", "listing_expiration_date": "20261231"}