# DULOXETINE HYDROCHLORIDE
> **ANDA090775** · Abbreviated New Drug Application (Generic) · Sponsor: SANDOZ · Approved 2011-02-02
## Drug
- **FDA Application Number:** ANDA090775
- **Application type:** Abbreviated New Drug Application (Generic)
- **Brand name:** DULOXETINE HYDROCHLORIDE
- **Generic name:** Duloxetine Hydrochloride
- **Active ingredients:** DULOXETINE HYDROCHLORIDE
- **Dosage form:** CAPSULE, DELAYED RELEASE
- **Route:** ORAL
- **Marketing status:** None (Tentative Approval)
- **Sponsor:** SANDOZ
- **First approval:** 2011-02-02
## Source
- [Drugs@FDA application overview](https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=090775)
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