Package 55154-0257-8

Brand: trintellix

Generic: vortioxetine
NDC Package

Package Facts

Identity

Package NDC 55154-0257-8
Digits Only 5515402578
Product NDC 55154-0257
Product ID 55154-0257_7b53e0ea-8161-474c-b623-734841128a9a
Description

2430 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55154-0257-8)

Marketing

Marketing Status
Marketed Since 2013-10-02
Brand trintellix
Generic vortioxetine
Sample Package No

Linked Drug Pages (1)

Trintellix ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "7b53e0ea-8161-474c-b623-734841128a9a", "openfda": {"upc": ["0355154025783", "0355154025684"], "unii": ["TKS641KOAY"], "rxcui": ["1439808", "1439810", "1790886", "1790890"], "spl_set_id": ["cb1e9df4-dd74-4073-9d78-bb55593dd000"], "manufacturer_name": ["Cardinal Health 107, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "2430 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55154-0257-8)", "package_ndc": "55154-0257-8", "marketing_start_date": "20131002"}], "brand_name": "Trintellix", "product_id": "55154-0257_7b53e0ea-8161-474c-b623-734841128a9a", "dosage_form": "TABLET, FILM COATED", "product_ndc": "55154-0257", "generic_name": "vortioxetine", "labeler_name": "Cardinal Health 107, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Trintellix", "active_ingredients": [{"name": "VORTIOXETINE HYDROBROMIDE", "strength": "20 mg/1"}], "application_number": "NDA204447", "marketing_category": "NDA", "marketing_start_date": "20131002", "listing_expiration_date": "20271231"}