Package 67877-736-05

{"route": ["ORAL"], "spl_id": "062a789f-52f0-482b-9ec0-2ba3ac1572ec", "openfda": {"nui": ["N0000008486"], "unii": ["563KS2PQY5"], "rxcui": ["809987", "809992", "809996", "810000"], "spl_set_id": ["9d7fde23-dc3f-41e9-89cf-6a1a9eeaa7de"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Ascend Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (67877-736-05)", "package_ndc": "67877-736-05", "marketing_start_date": "20220401"}, {"sample": false, "description": "6 BLISTER PACK in 1 CARTON (67877-736-31)  / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "67877-736-31", "marketing_start_date": "20220401"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (67877-736-60)", "package_ndc": "67877-736-60", "marketing_start_date": "20220401"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (67877-736-90)", "package_ndc": "67877-736-90", "marketing_start_date": "20220401"}], "brand_name": "Lacosamide", "product_id": "67877-736_062a789f-52f0-482b-9ec0-2ba3ac1572ec", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "67877-736", "dea_schedule": "CV", "generic_name": "Lacosamide", "labeler_name": "Ascend Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lacosamide", "active_ingredients": [{"name": "LACOSAMIDE", "strength": "200 mg/1"}], "application_number": "ANDA214695", "marketing_category": "ANDA", "marketing_start_date": "20220401", "listing_expiration_date": "20261231"}