Package 60687-698-57

Brand: lacosamide

Generic: lacosamide
NDC Package

Package Facts

Identity

Package NDC 60687-698-57
Digits Only 6068769857
Product NDC 60687-698
Description

60 BLISTER PACK in 1 CARTON (60687-698-57) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-698-11)

Marketing

Marketing Status
Marketed Since 2022-06-03
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": "25b624cd-41b3-7d05-e063-6294a90ab060", "openfda": {"nui": ["N0000008486"], "unii": ["563KS2PQY5"], "rxcui": ["809987", "809996", "810000"], "spl_set_id": ["19060029-c158-4a37-9261-cfe3b2b5b1e3"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "60 BLISTER PACK in 1 CARTON (60687-698-57)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-698-11)", "package_ndc": "60687-698-57", "marketing_start_date": "20220603"}], "brand_name": "Lacosamide", "product_id": "60687-698_25b624cd-41b3-7d05-e063-6294a90ab060", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "60687-698", "dea_schedule": "CV", "generic_name": "Lacosamide", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lacosamide", "active_ingredients": [{"name": "LACOSAMIDE", "strength": "200 mg/1"}], "application_number": "ANDA214695", "marketing_category": "ANDA", "marketing_start_date": "20220603", "listing_expiration_date": "20261231"}