# VORTIOXETINE
> **ANDA211024** · Abbreviated New Drug Application (Generic) · Sponsor: PRINSTON PHARMA INC · Approved 2022-07-28
## Drug
- **FDA Application Number:** ANDA211024
- **Application type:** Abbreviated New Drug Application (Generic)
- **Brand name:** VORTIOXETINE
- **Generic name:** Vortioxetine
- **Active ingredients:** VORTIOXETINE
- **Dosage form:** TABLET
- **Route:** ORAL
- **Marketing status:** None (Tentative Approval)
- **Sponsor:** PRINSTON PHARMA INC
- **First approval:** 2022-07-28
## Source
- [Drugs@FDA application overview](https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=211024)
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