Package 70771-1760-1

{"route": ["ORAL"], "spl_id": "9d6e36f0-a9e4-4b66-997a-fd5f8e4e1cf7", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH", "UR59KN573L"], "rxcui": ["854908", "854916", "854919"], "spl_set_id": ["35ed3030-a9b3-4e4e-99cd-6d5c31ad22fa"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (70771-1760-1)", "package_ndc": "70771-1760-1", "marketing_start_date": "20230301"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (70771-1760-3)", "package_ndc": "70771-1760-3", "marketing_start_date": "20230301"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (70771-1760-5)", "package_ndc": "70771-1760-5", "marketing_start_date": "20230301"}], "brand_name": "Bisoprolol Fumarate and Hydrochlorothiazide", "product_id": "70771-1760_9d6e36f0-a9e4-4b66-997a-fd5f8e4e1cf7", "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": "70771-1760", "generic_name": "bisoprolol fumarate and hydrochlorothiazide", "labeler_name": "Zydus Lifesciences Limited", "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": "ANDA215666", "marketing_category": "ANDA", "marketing_start_date": "20230301", "listing_expiration_date": "20261231"}