Package 50090-5905-0

{"route": ["ORAL"], "spl_id": "fe02e259-324e-4cee-9151-6c4711e2b507", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["UR59KN573L", "0J48LPH2TH"], "rxcui": ["854908"], "spl_set_id": ["6b7f96c3-daf4-4029-a96b-baa37add0edb"], "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 (50090-5905-0)", "package_ndc": "50090-5905-0", "marketing_start_date": "20220117"}], "brand_name": "Bisoprolol Fumarate and Hydrochlorothiazide", "product_id": "50090-5905_fe02e259-324e-4cee-9151-6c4711e2b507", "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": "50090-5905", "generic_name": "Bisoprolol Fumarate and Hydrochlorothiazide", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bisoprolol Fumarate and Hydrochlorothiazide", "active_ingredients": [{"name": "BISOPROLOL FUMARATE", "strength": "10 mg/1"}, {"name": "HYDROCHLOROTHIAZIDE", "strength": "6.25 mg/1"}], "application_number": "ANDA212678", "marketing_category": "ANDA", "marketing_start_date": "20190430", "listing_expiration_date": "20261231"}