Package 29300-364-05

{"route": ["ORAL"], "spl_id": "d452fee5-4940-4740-8c4d-8024788eafc6", "openfda": {"nui": ["N0000008486"], "unii": ["563KS2PQY5"], "rxcui": ["809987", "809992", "809996", "810000"], "spl_set_id": ["7ed5cebe-470e-48a4-86ec-2ce79cc32688"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Unichem Pharmaceuticals (USA), Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (29300-364-05)", "package_ndc": "29300-364-05", "marketing_start_date": "20241201"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (29300-364-16)", "package_ndc": "29300-364-16", "marketing_start_date": "20241201"}], "brand_name": "Lacosamide", "product_id": "29300-364_d452fee5-4940-4740-8c4d-8024788eafc6", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "29300-364", "dea_schedule": "CV", "generic_name": "Lacosamide", "labeler_name": "Unichem Pharmaceuticals (USA), Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lacosamide", "active_ingredients": [{"name": "LACOSAMIDE", "strength": "50 mg/1"}], "application_number": "ANDA213109", "marketing_category": "ANDA", "marketing_start_date": "20241201", "listing_expiration_date": "20261231"}