# Trintellix

NDC: 70518-4284
Generic name: vortioxetine
Labeler / Manufacturer: REMEDYREPACK INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20250211

FDA application: NDA204447

## Active ingredients

- VORTIOXETINE HYDROBROMIDE: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70518-4284"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70518-4284
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=239215eb-be32-4286-9677-1e5556c6cccf