Package 67046-1445-3
Brand: lacosamide
Generic: lacosamidePackage Facts
Identity
Package NDC
67046-1445-3
Digits Only
6704614453
Product NDC
67046-1445
Description
30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1445-3)
Marketing
Marketing Status
Brand
lacosamide
Generic
lacosamide
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2e969590-2f07-e068-e063-6294a90ab749", "openfda": {"nui": ["N0000008486"], "unii": ["563KS2PQY5"], "rxcui": ["809996"], "spl_set_id": ["2d999f1f-11c6-bc28-e063-6394a90a4a52"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1445-3)", "package_ndc": "67046-1445-3", "marketing_start_date": "20250207"}], "brand_name": "LACOSAMIDE", "product_id": "67046-1445_2e969590-2f07-e068-e063-6294a90ab749", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "67046-1445", "dea_schedule": "CV", "generic_name": "LACOSAMIDE", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LACOSAMIDE", "active_ingredients": [{"name": "LACOSAMIDE", "strength": "200 mg/1"}], "application_number": "ANDA204787", "marketing_category": "ANDA", "marketing_start_date": "20250207", "listing_expiration_date": "20261231"}