Package 68180-803-16

Brand: rufinamide

Generic: rufinamide
NDC Package

Package Facts

Identity

Package NDC 68180-803-16
Digits Only 6818080316
Product NDC 68180-803
Product ID 68180-803_3db88bc9-af10-4a67-86c5-9f034fa4db9a
Description

120 TABLET, FILM COATED in 1 BOTTLE (68180-803-16)

Marketing

Marketing Status
Marketed Since 2022-11-28
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": "3db88bc9-af10-4a67-86c5-9f034fa4db9a", "openfda": {"upc": ["0368180803164"], "unii": ["WFW942PR79"], "rxcui": ["824295", "824301", "2612668"], "spl_set_id": ["2c2c8d41-1ae4-453a-b628-954ee0b3be5c"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (68180-803-16)", "package_ndc": "68180-803-16", "marketing_start_date": "20221128"}], "brand_name": "RUFINAMIDE", "product_id": "68180-803_3db88bc9-af10-4a67-86c5-9f034fa4db9a", "dosage_form": "TABLET, FILM COATED", "product_ndc": "68180-803", "generic_name": "rufinamide", "labeler_name": "Lupin Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "RUFINAMIDE", "active_ingredients": [{"name": "RUFINAMIDE", "strength": "200 mg/1"}], "application_number": "ANDA204964", "marketing_category": "ANDA", "marketing_start_date": "20221128", "listing_expiration_date": "20261231"}