Package 0054-0425-23

Brand: rufinamide

Generic: rufinamide
NDC Package

Package Facts

Identity

Package NDC 0054-0425-23
Digits Only 0054042523
Product NDC 0054-0425
Product ID 0054-0425_72348f03-413e-4d00-be89-00c719af669b
Description

120 TABLET, FILM COATED in 1 BOTTLE (0054-0425-23)

Marketing

Marketing Status
Marketed Since 2021-05-30
Brand rufinamide
Generic rufinamide
Sample Package No

Linked Drug Pages (1)

Rufinamide ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "72348f03-413e-4d00-be89-00c719af669b", "openfda": {"upc": ["0300540425234", "0300540426231"], "unii": ["WFW942PR79"], "rxcui": ["824295", "824301"], "spl_set_id": ["56316809-6e73-4717-990b-fc84bf6bf433"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (0054-0425-23)", "package_ndc": "0054-0425-23", "marketing_start_date": "20210530"}], "brand_name": "Rufinamide", "product_id": "0054-0425_72348f03-413e-4d00-be89-00c719af669b", "dosage_form": "TABLET, FILM COATED", "product_ndc": "0054-0425", "generic_name": "Rufinamide", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Rufinamide", "active_ingredients": [{"name": "RUFINAMIDE", "strength": "200 mg/1"}], "application_number": "ANDA204988", "marketing_category": "ANDA", "marketing_start_date": "20210530", "listing_expiration_date": "20261231"}