# Trintellix

NDC: 64764-720
Generic name: vortioxetine
Labeler / Manufacturer: Takeda Pharmaceuticals America, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20131002

FDA application: NDA204447

## Active ingredients

- VORTIOXETINE HYDROBROMIDE: 5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"64764-720"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=64764-720
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1a5b68e2-14d0-419d-9ec6-1ca97145e838