Package 70518-4503-0

Brand: lacosamide

Generic: lacosamide
NDC Package

Package Facts

Identity

Package NDC 70518-4503-0
Digits Only 7051845030
Product NDC 70518-4503
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4503-0)

Marketing

Marketing Status
Marketed Since 2025-10-14
Brand lacosamide
Generic lacosamide
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "411fd337-46f4-8d47-e063-6394a90ac45d", "openfda": {"nui": ["N0000008486"], "unii": ["563KS2PQY5"], "rxcui": ["810000"], "spl_set_id": ["e3658b3c-f193-41a2-acc7-0bb912e27173"], "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 (70518-4503-0)", "package_ndc": "70518-4503-0", "marketing_start_date": "20251014"}], "brand_name": "Lacosamide", "product_id": "70518-4503_411fd337-46f4-8d47-e063-6394a90ac45d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "70518-4503", "dea_schedule": "CV", "generic_name": "lacosamide", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lacosamide", "active_ingredients": [{"name": "LACOSAMIDE", "strength": "50 mg/1"}], "application_number": "ANDA204974", "marketing_category": "ANDA", "marketing_start_date": "20251014", "listing_expiration_date": "20261231"}