# DULOXETINE HYDROCHLORIDE
> **ANDA207219** · Abbreviated New Drug Application (Generic) · Sponsor: YAOPHARMA CO LTD · Approved 2019-08-16
## Drug
- **FDA Application Number:** ANDA207219
- **Application type:** Abbreviated New Drug Application (Generic)
- **Brand name:** DULOXETINE HYDROCHLORIDE
- **Generic name:** DULOXETINE HYDROCHLORIDE
- **Active ingredients:** DULOXETINE HYDROCHLORIDE
- **Dosage form:** CAPSULE, DELAYED REL PELLETS
- **Route:** ORAL
- **Marketing status:** Discontinued
- **Sponsor:** YAOPHARMA CO LTD
- **Manufacturer:** Yaopharma Co., Ltd.
- **First approval:** 2019-08-16
## Source
- [Drugs@FDA application overview](https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=207219)
---
*MORVS · CC0 1.0*