# ATOMOXETINE HYDROCHLORIDE
> **ANDA079019** · Abbreviated New Drug Application (Generic) · Sponsor: GLENMARK PHARMS LTD · Approved 2017-05-30
## Drug
- **FDA Application Number:** ANDA079019
- **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:** GLENMARK PHARMS LTD
- **Manufacturer:** Northstar Rx LLC
- **First approval:** 2017-05-30
## Source
- [Drugs@FDA application overview](https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=079019)
---
*AI Analytics · CC0 1.0*