# ATOMOXETINE HYDROCHLORIDE
> **ANDA079017** · Abbreviated New Drug Application (Generic) · Sponsor: ZYDUS PHARMS USA INC · Approved 2010-09-16
## Drug
- **FDA Application Number:** ANDA079017
- **Application type:** Abbreviated New Drug Application (Generic)
- **Brand name:** ATOMOXETINE HYDROCHLORIDE
- **Generic name:** ATOMOXETINE
- **Active ingredients:** ATOMOXETINE HYDROCHLORIDE
- **Dosage form:** CAPSULE
- **Route:** ORAL
- **Marketing status:** Prescription
- **Sponsor:** ZYDUS PHARMS USA INC
- **Manufacturer:** Zydus Pharmaceuticals USA Inc.
- **First approval:** 2010-09-16
## Source
- [Drugs@FDA application overview](https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=079017)
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