Package 46708-403-30

{"route": ["ORAL"], "spl_id": "0bd202e3-c673-4945-b828-1a5bc6a896ae", "openfda": {"nui": ["N0000000161", "N0000175556"], "upc": ["0346708403300", "0346708402303", "0346708404307"], "unii": ["FEN504330V"], "rxcui": ["198006", "198007", "198008"], "spl_set_id": ["0bd202e3-c673-4945-b828-1a5bc6a896ae"], "pharm_class_epc": ["beta-Adrenergic Blocker [EPC]"], "pharm_class_moa": ["Adrenergic beta-Antagonists [MoA]"], "manufacturer_name": ["Alembic Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (46708-403-30)", "package_ndc": "46708-403-30", "marketing_start_date": "20230608"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (46708-403-31)", "package_ndc": "46708-403-31", "marketing_start_date": "20230608"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (46708-403-91)", "package_ndc": "46708-403-91", "marketing_start_date": "20230608"}], "brand_name": "NADOLOL", "product_id": "46708-403_0bd202e3-c673-4945-b828-1a5bc6a896ae", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "46708-403", "generic_name": "NADOLOL", "labeler_name": "Alembic Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "NADOLOL", "active_ingredients": [{"name": "NADOLOL", "strength": "40 mg/1"}], "application_number": "ANDA211763", "marketing_category": "ANDA", "marketing_start_date": "20230608", "listing_expiration_date": "20261231"}