Package 31722-599-30

Brand: rufinamide

Generic: rufinamide
NDC Package

Package Facts

Identity

Package NDC 31722-599-30
Digits Only 3172259930
Product NDC 31722-599
Description

30 TABLET, FILM COATED in 1 BOTTLE (31722-599-30)

Marketing

Marketing Status
Marketed Since 2021-05-11
Brand rufinamide
Generic rufinamide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "c3c611a2-394b-4427-e053-2a95a90a433f", "openfda": {"upc": ["0331722599122", "0331722598125"], "unii": ["WFW942PR79"], "rxcui": ["824295", "824301"], "spl_set_id": ["afe24968-e078-46d6-a776-b2608734e03e"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (31722-599-12)", "package_ndc": "31722-599-12", "marketing_start_date": "20210511"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (31722-599-30)", "package_ndc": "31722-599-30", "marketing_start_date": "20210511"}], "brand_name": "Rufinamide", "product_id": "31722-599_c3c611a2-394b-4427-e053-2a95a90a433f", "dosage_form": "TABLET, FILM COATED", "product_ndc": "31722-599", "generic_name": "Rufinamide", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Rufinamide", "active_ingredients": [{"name": "RUFINAMIDE", "strength": "400 mg/1"}], "application_number": "ANDA204993", "marketing_category": "ANDA", "marketing_start_date": "20210511", "listing_expiration_date": "20261231"}