# VORTIOXETINE HYDROBROMIDE
> **ANDA211146** · Abbreviated New Drug Application (Generic) · Sponsor: ZYDUS PHARMS · Approved 2024-04-02
## Drug
- **FDA Application Number:** ANDA211146
- **Application type:** Abbreviated New Drug Application (Generic)
- **Brand name:** VORTIOXETINE HYDROBROMIDE
- **Generic name:** Vortioxetine Hydrobromide
- **Active ingredients:** VORTIOXETINE HYDROBROMIDE
- **Dosage form:** TABLET
- **Route:** ORAL
- **Marketing status:** Discontinued
- **Sponsor:** ZYDUS PHARMS
- **First approval:** 2024-04-02
## Source
- [Drugs@FDA application overview](https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=211146)
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