Package 72205-038-77

Brand: rufinamide

Generic: rufinamide
NDC Package

Package Facts

Identity

Package NDC 72205-038-77
Digits Only 7220503877
Product NDC 72205-038
Description

1 BOTTLE in 1 CARTON (72205-038-77) / 460 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2025-06-01
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": "924ffdf9-ce5f-4989-9a43-78a03ba3eaed", "openfda": {"unii": ["WFW942PR79"], "rxcui": ["1092357"], "spl_set_id": ["924ffdf9-ce5f-4989-9a43-78a03ba3eaed"], "manufacturer_name": ["Novadoz Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (72205-038-77)  / 460 mL in 1 BOTTLE", "package_ndc": "72205-038-77", "marketing_start_date": "20250601"}], "brand_name": "Rufinamide", "product_id": "72205-038_924ffdf9-ce5f-4989-9a43-78a03ba3eaed", "dosage_form": "SUSPENSION", "product_ndc": "72205-038", "generic_name": "Rufinamide", "labeler_name": "Novadoz Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Rufinamide", "active_ingredients": [{"name": "RUFINAMIDE", "strength": "40 mg/mL"}], "application_number": "ANDA214817", "marketing_category": "ANDA", "marketing_start_date": "20250415", "listing_expiration_date": "20261231"}