Package 62856-582-52

Brand: banzel

Generic: rufinamide
NDC Package

Package Facts

Identity

Package NDC 62856-582-52
Digits Only 6285658252
Product NDC 62856-582
Description

120 TABLET, FILM COATED in 1 BOTTLE (62856-582-52)

Marketing

Marketing Status
Marketed Since 2008-11-14
Brand banzel
Generic rufinamide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0cc6f13a-0289-45f7-980e-3196d7489d75", "openfda": {"upc": ["0362856584463", "0362856582520"], "unii": ["WFW942PR79"], "rxcui": ["824295", "824299", "824301", "824303", "1092357", "1092360"], "spl_set_id": ["0a3fa925-1abd-458a-bd57-4ae780a1ef2d"], "manufacturer_name": ["Eisai Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": true, "description": "4 TABLET, FILM COATED in 1 BOTTLE (62856-582-04)", "package_ndc": "62856-582-04", "marketing_start_date": "20180808"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (62856-582-52)", "package_ndc": "62856-582-52", "marketing_start_date": "20081114"}], "brand_name": "Banzel", "product_id": "62856-582_0cc6f13a-0289-45f7-980e-3196d7489d75", "dosage_form": "TABLET, FILM COATED", "product_ndc": "62856-582", "generic_name": "rufinamide", "labeler_name": "Eisai Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Banzel", "active_ingredients": [{"name": "RUFINAMIDE", "strength": "200 mg/1"}], "application_number": "NDA021911", "marketing_category": "NDA", "marketing_start_date": "20081114", "listing_expiration_date": "20261231"}