Package 71335-2443-2

{"route": ["ORAL"], "spl_id": "3e583d86-66cb-4a0f-a868-416721f24ad1", "openfda": {"nui": ["N0000000161", "N0000175556"], "unii": ["030Y90569U"], "rxcui": ["751612"], "spl_set_id": ["78c0945a-b8dc-4397-95d5-9f209224ad5e"], "pharm_class_epc": ["beta-Adrenergic Blocker [EPC]"], "pharm_class_moa": ["Adrenergic beta-Antagonists [MoA]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-2443-1)", "package_ndc": "71335-2443-1", "marketing_start_date": "20240815"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-2443-2)", "package_ndc": "71335-2443-2", "marketing_start_date": "20240815"}], "brand_name": "NEBIVOLOL", "product_id": "71335-2443_3e583d86-66cb-4a0f-a868-416721f24ad1", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "71335-2443", "generic_name": "nebibolol", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "NEBIVOLOL", "active_ingredients": [{"name": "NEBIVOLOL", "strength": "10 mg/1"}], "application_number": "ANDA212682", "marketing_category": "ANDA", "marketing_start_date": "20220214", "listing_expiration_date": "20261231"}