Package 80005-118-11

{"route": ["ORAL"], "spl_id": "1f77f842-e0b6-4659-beee-0bb01da839e3", "openfda": {"nui": ["N0000175753", "N0000008486"], "unii": ["13AFD7670Q"], "rxcui": ["96304", "198150"], "spl_set_id": ["dc018b1d-72d3-45a2-84ff-cf9499c7ae97"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "pharm_class_epc": ["Anti-epileptic Agent [EPC]"], "manufacturer_name": ["Carnegie Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (80005-118-11)", "package_ndc": "80005-118-11", "marketing_start_date": "20240501"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (80005-118-14)", "package_ndc": "80005-118-14", "marketing_start_date": "20240501"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (80005-118-15)", "package_ndc": "80005-118-15", "marketing_start_date": "20240501"}], "brand_name": "Primidone", "product_id": "80005-118_1f77f842-e0b6-4659-beee-0bb01da839e3", "dosage_form": "TABLET", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "80005-118", "generic_name": "Primidone", "labeler_name": "Carnegie Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Primidone", "active_ingredients": [{"name": "PRIMIDONE", "strength": "250 mg/1"}], "application_number": "ANDA218366", "marketing_category": "ANDA", "marketing_start_date": "20240501", "listing_expiration_date": "20261231"}