# METHYLPHENIDATE HYDROCHLORIDE
> **ANDA214202** · Abbreviated New Drug Application (Generic) · Sponsor: TEVA PHARMS USA · Approved 2023-02-07
## Drug
- **FDA Application Number:** ANDA214202
- **Application type:** Abbreviated New Drug Application (Generic)
- **Brand name:** METHYLPHENIDATE HYDROCHLORIDE
- **Generic name:** Methylphenidate Hydrochloride
- **Active ingredients:** METHYLPHENIDATE HYDROCHLORIDE
- **Dosage form:** TABLET, EXTENDED RELEASE, CHEWABLE
- **Route:** ORAL
- **Marketing status:** None (Tentative Approval)
- **Sponsor:** TEVA PHARMS USA
- **First approval:** 2023-02-07
## Source
- [Drugs@FDA application overview](https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=214202)
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