Package 72603-261-01
Brand: rufinamide
Generic: rufinamidePackage Facts
Identity
Package NDC
72603-261-01
Digits Only
7260326101
Product NDC
72603-261
Description
1 BOTTLE in 1 CARTON (72603-261-01) / 460 mL in 1 BOTTLE
Marketing
Marketing Status
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": "1ccfda8b-0fa1-6b4a-e063-6294a90a15ad", "openfda": {"upc": ["0372603261011"], "unii": ["WFW942PR79"], "rxcui": ["1092357"], "spl_set_id": ["b682021c-74c3-4cc8-84af-acd94438397a"], "manufacturer_name": ["NorthStar RxLLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (72603-261-01) / 460 mL in 1 BOTTLE", "package_ndc": "72603-261-01", "marketing_start_date": "20240801"}], "brand_name": "Rufinamide", "product_id": "72603-261_1ccfda8b-0fa1-6b4a-e063-6294a90a15ad", "dosage_form": "SUSPENSION", "product_ndc": "72603-261", "generic_name": "Rufinamide", "labeler_name": "NorthStar RxLLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Rufinamide", "active_ingredients": [{"name": "RUFINAMIDE", "strength": "40 mg/mL"}], "application_number": "ANDA216841", "marketing_category": "ANDA", "marketing_start_date": "20240801", "listing_expiration_date": "20261231"}