Package 71335-2589-4

{"route": ["ORAL"], "spl_id": "f8af595c-3cbc-4e89-b7c8-1ab33290711a", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["UR59KN573L", "0J48LPH2TH"], "rxcui": ["854919"], "spl_set_id": ["794d4a5a-de31-4878-95d5-23552dd2171e"], "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 (71335-2589-1)", "package_ndc": "71335-2589-1", "marketing_start_date": "20250604"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-2589-2)", "package_ndc": "71335-2589-2", "marketing_start_date": "20250604"}, {"sample": false, "description": "28 TABLET, FILM COATED in 1 BOTTLE (71335-2589-3)", "package_ndc": "71335-2589-3", "marketing_start_date": "20250604"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (71335-2589-4)", "package_ndc": "71335-2589-4", "marketing_start_date": "20250604"}], "brand_name": "Bisoprolol Fumarate and Hydrochlorothiazide", "product_id": "71335-2589_f8af595c-3cbc-4e89-b7c8-1ab33290711a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "71335-2589", "generic_name": "Bisoprolol Fumarate and Hydrochlorothiazide", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bisoprolol Fumarate and Hydrochlorothiazide", "active_ingredients": [{"name": "BISOPROLOL FUMARATE", "strength": "5 mg/1"}, {"name": "HYDROCHLOROTHIAZIDE", "strength": "6.25 mg/1"}], "application_number": "ANDA215995", "marketing_category": "ANDA", "marketing_start_date": "20220126", "listing_expiration_date": "20261231"}