# DULOXETINE HYDROCHLORIDE
> **ANDA208706** · Abbreviated New Drug Application (Generic) · Sponsor: AJANTA PHARMA LTD · Approved 2017-01-06
## Drug
- **FDA Application Number:** ANDA208706
- **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:** AJANTA PHARMA LTD
- **Manufacturer:** Quallent Pharmaceuticals Health LLC
- **First approval:** 2017-01-06
## Source
- [Drugs@FDA application overview](https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=208706)
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