Package 69452-223-84

Brand: rufinamide

Generic: rufinamide
NDC Package

Package Facts

Identity

Package NDC 69452-223-84
Digits Only 6945222384
Product NDC 69452-223
Product ID 69452-223_3d338656-9665-cc13-e063-6294a90ab433
Description

1 BOTTLE in 1 CARTON (69452-223-84) / 460 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2020-11-06
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": "3d338656-9665-cc13-e063-6294a90ab433", "openfda": {"upc": ["0369452223840"], "unii": ["WFW942PR79"], "rxcui": ["1092357"], "spl_set_id": ["e2ba061a-49f0-4330-b0f0-00f2c3725625"], "manufacturer_name": ["Bionpharma Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (69452-223-84)  / 460 mL in 1 BOTTLE", "package_ndc": "69452-223-84", "marketing_start_date": "20201106"}], "brand_name": "Rufinamide", "product_id": "69452-223_3d338656-9665-cc13-e063-6294a90ab433", "dosage_form": "SUSPENSION", "product_ndc": "69452-223", "generic_name": "Rufinamide", "labeler_name": "Bionpharma Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Rufinamide", "active_ingredients": [{"name": "RUFINAMIDE", "strength": "40 mg/mL"}], "application_number": "ANDA211388", "marketing_category": "ANDA", "marketing_start_date": "20181219", "listing_expiration_date": "20261231"}