Package 42571-391-12

Brand: rufinamide

Generic: rufinamide
NDC Package

Package Facts

Identity

Package NDC 42571-391-12
Digits Only 4257139112
Product NDC 42571-391
Product ID 42571-391_fbdca190-53fc-29e9-e053-6394a90abafe
Description

120 TABLET in 1 BOTTLE (42571-391-12)

Marketing

Marketing Status
Marketed Since 2023-07-01
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": "fbdca190-53fc-29e9-e053-6394a90abafe", "openfda": {"upc": ["0342571391126", "0342571392123"], "unii": ["WFW942PR79"], "rxcui": ["824295", "824301"], "spl_set_id": ["12fc41f9-b6a9-4bbd-afbe-5d269f5a42f6"], "manufacturer_name": ["Micro Labs Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET in 1 BOTTLE (42571-391-12)", "package_ndc": "42571-391-12", "marketing_start_date": "20230701"}], "brand_name": "RUFINAMIDE", "product_id": "42571-391_fbdca190-53fc-29e9-e053-6394a90abafe", "dosage_form": "TABLET", "product_ndc": "42571-391", "generic_name": "RUFINAMIDE", "labeler_name": "Micro Labs Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "RUFINAMIDE", "active_ingredients": [{"name": "RUFINAMIDE", "strength": "200 mg/1"}], "application_number": "ANDA216688", "marketing_category": "ANDA", "marketing_start_date": "20230701", "listing_expiration_date": "20261231"}