Package 51991-349-06

Brand: lacosamide

Generic: lacosamide
NDC Package

Package Facts

Identity

Package NDC 51991-349-06
Digits Only 5199134906
Product NDC 51991-349
Product ID 51991-349_d59d1657-c847-475f-998d-49d186f6697e
Description

60 TABLET, FILM COATED in 1 BOTTLE (51991-349-06)

Marketing

Marketing Status
Marketed Since 2022-03-18
Brand lacosamide
Generic lacosamide
Sample Package No

Linked Drug Pages (1)

LACOSAMIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "d59d1657-c847-475f-998d-49d186f6697e", "openfda": {"nui": ["N0000008486"], "unii": ["563KS2PQY5"], "rxcui": ["809987", "809992", "809996", "810000"], "spl_set_id": ["f7ea3ce6-4ca7-4405-a011-48e7d71360a5"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Breckenridge Pharmaceutical, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (51991-349-05)", "package_ndc": "51991-349-05", "marketing_start_date": "20220318"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (51991-349-06)", "package_ndc": "51991-349-06", "marketing_start_date": "20220318"}], "brand_name": "LACOSAMIDE", "product_id": "51991-349_d59d1657-c847-475f-998d-49d186f6697e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "51991-349", "dea_schedule": "CV", "generic_name": "LACOSAMIDE", "labeler_name": "Breckenridge Pharmaceutical, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LACOSAMIDE", "active_ingredients": [{"name": "LACOSAMIDE", "strength": "100 mg/1"}], "application_number": "ANDA204921", "marketing_category": "ANDA", "marketing_start_date": "20220318", "listing_expiration_date": "20261231"}