Package 68180-797-01

Brand: rufinamide

Generic: rufinamide
NDC Package

Package Facts

Identity

Package NDC 68180-797-01
Digits Only 6818079701
Product NDC 68180-797
Description

1 BOTTLE in 1 CARTON (68180-797-01) / 460 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2023-06-22
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": "47c9752b-a06d-46af-a029-9213e2474378", "openfda": {"upc": ["0368180797012"], "unii": ["WFW942PR79"], "rxcui": ["1092357"], "spl_set_id": ["1e671632-d5bd-499a-ba06-0d1dc0d99622"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (68180-797-01)  / 460 mL in 1 BOTTLE", "package_ndc": "68180-797-01", "marketing_start_date": "20230622"}], "brand_name": "Rufinamide", "product_id": "68180-797_47c9752b-a06d-46af-a029-9213e2474378", "dosage_form": "SUSPENSION", "product_ndc": "68180-797", "generic_name": "Rufinamide", "labeler_name": "Lupin Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Rufinamide", "active_ingredients": [{"name": "RUFINAMIDE", "strength": "40 mg/mL"}], "application_number": "ANDA213457", "marketing_category": "ANDA", "marketing_start_date": "20230622", "listing_expiration_date": "20261231"}