trintellix

Generic: vortioxetine

Labeler: cardinal health 107, llc
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name trintellix
Generic Name vortioxetine
Labeler cardinal health 107, llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

vortioxetine hydrobromide 20 mg/1

Manufacturer
Cardinal Health 107, LLC

Identifiers & Regulatory

Product NDC 55154-0257
Product ID 55154-0257_7b53e0ea-8161-474c-b623-734841128a9a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA204447
Listing Expiration 2027-12-31
Marketing Start 2013-10-02

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 551540257
Hyphenated Format 55154-0257

Supplemental Identifiers

RxCUI
1439808 1439810 1790886 1790890
UPC
0355154025783 0355154025684
UNII
TKS641KOAY

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name trintellix (source: ndc)
Generic Name vortioxetine (source: ndc)
Application Number NDA204447 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 2430 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55154-0257-8)
source: ndc

Packages (1)

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

Ingredients (1)

vortioxetine hydrobromide (20 mg/1)

Linked Drug Pages (1)

Trintellix ndc-match (0.9)

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"}