Package 0093-3243-56

{"route": ["ORAL"], "spl_id": "e67411e1-0823-4876-a456-cbf397c24086", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0300933241014", "0300933243568"], "unii": ["0J48LPH2TH", "UR59KN573L"], "rxcui": ["854908", "854916", "854919"], "spl_set_id": ["27d52b23-e3e2-4339-b00e-cd0fec43ffbb"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (0093-3243-56)", "package_ndc": "0093-3243-56", "marketing_start_date": "20190807"}], "brand_name": "bisoprolol fumarate and hydrochlorothiazide", "product_id": "0093-3243_e67411e1-0823-4876-a456-cbf397c24086", "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": "0093-3243", "generic_name": "bisoprolol fumarate and hydrochlorothiazide", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "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": "NDA020186", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20190807", "listing_expiration_date": "20261231"}