Package 71335-0845-3

{"route": ["ORAL"], "spl_id": "485df23f-178f-4ad2-b995-d31af927c845", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH", "6M97XTV3HD"], "rxcui": ["403854"], "spl_set_id": ["0360db3a-17cf-4d24-97ba-e0a6fcc94351"], "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 (71335-0845-1)", "package_ndc": "71335-0845-1", "marketing_start_date": "20240529"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-0845-2)", "package_ndc": "71335-0845-2", "marketing_start_date": "20180531"}, {"sample": false, "description": "28 TABLET, FILM COATED in 1 BOTTLE (71335-0845-3)", "package_ndc": "71335-0845-3", "marketing_start_date": "20240529"}], "brand_name": "Olmesartan Medoxomil and Hydrochlorothiazide", "product_id": "71335-0845_485df23f-178f-4ad2-b995-d31af927c845", "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": "71335-0845", "generic_name": "Olmesartan Medoxomil and Hydrochlorothiazide", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olmesartan Medoxomil and Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "12.5 mg/1"}, {"name": "OLMESARTAN MEDOXOMIL", "strength": "40 mg/1"}], "application_number": "ANDA205391", "marketing_category": "ANDA", "marketing_start_date": "20170424", "listing_expiration_date": "20261231"}