# DEXMETHYLPHENIDATE HYDROCHLORIDE
> **ANDA202731** · Abbreviated New Drug Application (Generic) · Sponsor: TEVA PHARMS USA · Approved 2014-05-19
## Drug
- **FDA Application Number:** ANDA202731
- **Application type:** Abbreviated New Drug Application (Generic)
- **Brand name:** DEXMETHYLPHENIDATE HYDROCHLORIDE
- **Generic name:** DEXMETHYLPHENIDATE HYDROCHLORIDE
- **Active ingredients:** DEXMETHYLPHENIDATE HYDROCHLORIDE
- **Dosage form:** CAPSULE, EXTENDED RELEASE
- **Route:** ORAL
- **Marketing status:** Prescription
- **Sponsor:** TEVA PHARMS USA
- **Manufacturer:** Teva Pharmaceuticals USA, Inc.
- **First approval:** 2014-05-19
## Source
- [Drugs@FDA application overview](https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=202731)
---
*MORVS · CC0 1.0*