Package 70518-4561-0

Brand: lacosamide

Generic: lacosamide
NDC Package

Package Facts

Identity

Package NDC 70518-4561-0
Digits Only 7051845610
Product NDC 70518-4561
Description

30 POUCH in 1 BOX (70518-4561-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-4561-1)

Marketing

Marketing Status
Marketed Since 2026-02-02
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": "49eba818-10bc-8c76-e063-6394a90a3e82", "openfda": {"nui": ["N0000008486"], "unii": ["563KS2PQY5"], "rxcui": ["809987"], "spl_set_id": ["8d2906e3-d059-425d-b971-29423963c2af"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 POUCH in 1 BOX (70518-4561-0)  / 1 TABLET, FILM COATED in 1 POUCH (70518-4561-1)", "package_ndc": "70518-4561-0", "marketing_start_date": "20260202"}], "brand_name": "Lacosamide", "product_id": "70518-4561_49eba818-10bc-8c76-e063-6394a90a3e82", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "70518-4561", "dea_schedule": "CV", "generic_name": "Lacosamide", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lacosamide", "active_ingredients": [{"name": "LACOSAMIDE", "strength": "100 mg/1"}], "application_number": "ANDA214695", "marketing_category": "ANDA", "marketing_start_date": "20260202", "listing_expiration_date": "20271231"}