Package 42799-920-01

{"route": ["ORAL"], "spl_id": "46410e5f-f09f-62ff-e063-6394a90afdda", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0342799922300", "0342799921020", "0342799921013", "0342799921303", "0342799920306", "0342799922027", "0342799920016", "0342799920023"], "unii": ["0J48LPH2TH", "UR59KN573L"], "rxcui": ["854908", "854916", "854919"], "spl_set_id": ["295532b5-65c8-40c3-8d27-cfd334d12802"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Edenbridge Pharmaceuticals LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (42799-920-01)", "package_ndc": "42799-920-01", "marketing_start_date": "20190430"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (42799-920-02)", "package_ndc": "42799-920-02", "marketing_start_date": "20190430"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (42799-920-30)", "package_ndc": "42799-920-30", "marketing_start_date": "20190430"}], "brand_name": "Bisoprolol Fumarate and Hydrochlorothiazide", "product_id": "42799-920_46410e5f-f09f-62ff-e063-6394a90afdda", "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": "42799-920", "generic_name": "Bisoprolol Fumarate and Hydrochlorothiazide", "labeler_name": "Edenbridge Pharmaceuticals LLC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bisoprolol Fumarate and Hydrochlorothiazide", "active_ingredients": [{"name": "BISOPROLOL FUMARATE", "strength": "2.5 mg/1"}, {"name": "HYDROCHLOROTHIAZIDE", "strength": "6.25 mg/1"}], "application_number": "ANDA212678", "marketing_category": "ANDA", "marketing_start_date": "20190430", "listing_expiration_date": "20261231"}