Package 70518-4505-0

Brand: lacosamide

Generic: lacosamide
NDC Package

Package Facts

Identity

Package NDC 70518-4505-0
Digits Only 7051845050
Product NDC 70518-4505
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4505-0)

Marketing

Marketing Status
Marketed Since 2025-10-14
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": "4120061a-dbb2-8918-e063-6394a90afbf2", "openfda": {"nui": ["N0000008486"], "unii": ["563KS2PQY5"], "rxcui": ["809987"], "spl_set_id": ["ae9f4f1b-574d-4c9a-80cb-189ccb232723"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4505-0)", "package_ndc": "70518-4505-0", "marketing_start_date": "20251014"}], "brand_name": "Lacosamide", "product_id": "70518-4505_4120061a-dbb2-8918-e063-6394a90afbf2", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "70518-4505", "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": "ANDA204974", "marketing_category": "ANDA", "marketing_start_date": "20251014", "listing_expiration_date": "20261231"}