# DEXMETHYLPHENIDATE HYDROCHLORIDE
> **ANDA206734** · Abbreviated New Drug Application (Generic) · Sponsor: SUN PHARM INDS INC · Approved 2021-11-05
## Drug
- **FDA Application Number:** ANDA206734
- **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:** Discontinued
- **Sponsor:** SUN PHARM INDS INC
- **First approval:** 2021-11-05
## Source
- [Drugs@FDA application overview](https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=206734)
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