Package 80425-0510-1

{"route": ["ORAL"], "spl_id": "325df1f8-167c-c07c-e063-6294a90a96fb", "openfda": {"nui": ["N0000008486"], "unii": ["563KS2PQY5"], "rxcui": ["810000"], "spl_set_id": ["325df1b7-4908-0c03-e063-6294a90ad844"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (80425-0510-1)", "package_ndc": "80425-0510-1", "marketing_start_date": "20250409"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (80425-0510-2)", "package_ndc": "80425-0510-2", "marketing_start_date": "20250409"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (80425-0510-3)", "package_ndc": "80425-0510-3", "marketing_start_date": "20250409"}], "brand_name": "Lacosamide", "product_id": "80425-0510_325df1f8-167c-c07c-e063-6294a90a96fb", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "80425-0510", "dea_schedule": "CV", "generic_name": "Lacosamide", "labeler_name": "Advanced Rx of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lacosamide", "active_ingredients": [{"name": "LACOSAMIDE", "strength": "50 mg/1"}], "application_number": "ANDA214695", "marketing_category": "ANDA", "marketing_start_date": "20250409", "listing_expiration_date": "20261231"}