Package 68462-713-08

Brand: rufinamide

Generic: rufinamide
NDC Package

Package Facts

Identity

Package NDC 68462-713-08
Digits Only 6846271308
Product NDC 68462-713
Description

120 TABLET, FILM COATED in 1 BOTTLE (68462-713-08)

Marketing

Marketing Status
Marketed Since 2016-05-16
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": "18421d5f-9e93-4abb-8abe-855bab5d243e", "openfda": {"upc": ["0368462714089", "0368462713082"], "unii": ["WFW942PR79"], "rxcui": ["824295", "824301"], "spl_set_id": ["da9ee326-a383-4d46-9d4e-fcc2be3d2680"], "manufacturer_name": ["Glenmark Pharmaceuticals Inc., USA"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (68462-713-05)", "package_ndc": "68462-713-05", "marketing_start_date": "20160516"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (68462-713-08)", "package_ndc": "68462-713-08", "marketing_start_date": "20160516"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68462-713-30)", "package_ndc": "68462-713-30", "marketing_start_date": "20160516"}], "brand_name": "rufinamide", "product_id": "68462-713_18421d5f-9e93-4abb-8abe-855bab5d243e", "dosage_form": "TABLET, FILM COATED", "product_ndc": "68462-713", "generic_name": "rufinamide", "labeler_name": "Glenmark Pharmaceuticals Inc., USA", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "rufinamide", "active_ingredients": [{"name": "RUFINAMIDE", "strength": "200 mg/1"}], "application_number": "ANDA205075", "marketing_category": "ANDA", "marketing_start_date": "20160516", "listing_expiration_date": "20271231"}