Package 59651-617-08

Brand: rufinamide

Generic: rufinamide
NDC Package

Package Facts

Identity

Package NDC 59651-617-08
Digits Only 5965161708
Product NDC 59651-617
Product ID 59651-617_96d61d77-4de0-4c57-997d-014010177a86
Description

120 TABLET, FILM COATED in 1 BOTTLE (59651-617-08)

Marketing

Marketing Status
Marketed Since 2023-06-16
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": "96d61d77-4de0-4c57-997d-014010177a86", "openfda": {"upc": ["0359651616086"], "unii": ["WFW942PR79"], "rxcui": ["824295", "824301"], "spl_set_id": ["d9ffc833-d902-41cb-8e8e-6bbba8e65b9e"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (59651-617-08)", "package_ndc": "59651-617-08", "marketing_start_date": "20230616"}], "brand_name": "Rufinamide", "product_id": "59651-617_96d61d77-4de0-4c57-997d-014010177a86", "dosage_form": "TABLET, FILM COATED", "product_ndc": "59651-617", "generic_name": "rufinamide", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Rufinamide", "active_ingredients": [{"name": "RUFINAMIDE", "strength": "400 mg/1"}], "application_number": "ANDA217230", "marketing_category": "ANDA", "marketing_start_date": "20230616", "listing_expiration_date": "20261231"}