# ATOMOXETINE HYDROCHLORIDE
> **ANDA079020** · Abbreviated New Drug Application (Generic) · Sponsor: SUN PHARMA GLOBAL · Approved 2012-05-11
## Drug
- **FDA Application Number:** ANDA079020
- **Application type:** Abbreviated New Drug Application (Generic)
- **Brand name:** ATOMOXETINE HYDROCHLORIDE
- **Generic name:** Atomoxetine Hydrochloride
- **Active ingredients:** ATOMOXETINE HYDROCHLORIDE
- **Dosage form:** CAPSULE
- **Route:** ORAL
- **Marketing status:** None (Tentative Approval)
- **Sponsor:** SUN PHARMA GLOBAL
- **First approval:** 2012-05-11
## Source
- [Drugs@FDA application overview](https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=079020)
---
*MORVS · CC0 1.0*