# DULOXETINE HYDROCHLORIDE
> **ANDA204343** · Abbreviated New Drug Application (Generic) · Sponsor: HETERO LABS LTD III · Approved 2016-08-03
## Drug
- **FDA Application Number:** ANDA204343
- **Application type:** Abbreviated New Drug Application (Generic)
- **Brand name:** DULOXETINE HYDROCHLORIDE
- **Generic name:** DULOXETINE
- **Active ingredients:** DULOXETINE HYDROCHLORIDE
- **Dosage form:** CAPSULE, DELAYED REL PELLETS
- **Route:** ORAL
- **Marketing status:** Prescription
- **Sponsor:** HETERO LABS LTD III
- **Manufacturer:** Camber Pharmaceuticals, Inc.
- **First approval:** 2016-08-03
## Source
- [Drugs@FDA application overview](https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=204343)
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