Package 50228-193-60

Brand: lacosamide

Generic: lacosamide
NDC Package

Package Facts

Identity

Package NDC 50228-193-60
Digits Only 5022819360
Product NDC 50228-193
Description

60 TABLET, FILM COATED in 1 BOTTLE (50228-193-60)

Marketing

Marketing Status
Marketed Since 2022-03-18
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": "56788345-3f8e-478c-b73d-216b4d711b57", "openfda": {"nui": ["N0000008486"], "upc": ["0350228195607", "0350228193603", "0350228194600", "0350228192606"], "unii": ["563KS2PQY5"], "rxcui": ["809987", "809992", "809996", "810000"], "spl_set_id": ["f4ffa3ad-1278-4772-9ef8-ed6fdaa47605"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["ScieGen Pharmaceuticals Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (50228-193-10)", "package_ndc": "50228-193-10", "marketing_start_date": "20220318"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50228-193-30)", "package_ndc": "50228-193-30", "marketing_start_date": "20220318"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (50228-193-60)", "package_ndc": "50228-193-60", "marketing_start_date": "20220318"}], "brand_name": "LACOSAMIDE", "product_id": "50228-193_56788345-3f8e-478c-b73d-216b4d711b57", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "50228-193", "dea_schedule": "CV", "generic_name": "LACOSAMIDE", "labeler_name": "ScieGen Pharmaceuticals Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LACOSAMIDE", "active_ingredients": [{"name": "LACOSAMIDE", "strength": "100 mg/1"}], "application_number": "ANDA205237", "marketing_category": "ANDA", "marketing_start_date": "20220318", "listing_expiration_date": "20261231"}