Package 71335-3048-1

{"route": ["ORAL"], "spl_id": "c5d89e5e-c542-4ae0-af2d-3f546fd2bb39", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH", "3ST302B24A"], "rxcui": ["979464"], "spl_set_id": ["f5f462c6-0604-49d3-af8f-fecbde23be99"], "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": "1000 TABLET, FILM COATED in 1 BOTTLE (71335-3048-1)", "package_ndc": "71335-3048-1", "marketing_start_date": "20251203"}], "brand_name": "Losartan potassium and Hydrochlorothiazide", "product_id": "71335-3048_c5d89e5e-c542-4ae0-af2d-3f546fd2bb39", "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": "71335-3048", "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": "ANDA202289", "marketing_category": "ANDA", "marketing_start_date": "20120503", "listing_expiration_date": "20261231"}