# DULOXETINE HYDROCHLORIDE
> **ANDA203088** · Abbreviated New Drug Application (Generic) · Sponsor: BRECKENRIDGE · Approved 2014-06-11
## Drug
- **FDA Application Number:** ANDA203088
- **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:** Prescription
- **Sponsor:** BRECKENRIDGE
- **Manufacturer:** Breckenridge Pharmaceutical, Inc.
- **First approval:** 2014-06-11
## Source
- [Drugs@FDA application overview](https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=203088)
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