# DEXMETHYLPHENIDATE HYDROCHLORIDE
> **ANDA201231** · Abbreviated New Drug Application (Generic) · Sponsor: SUN PHARM INDUSTRIES · Approved 2015-09-24
## Drug
- **FDA Application Number:** ANDA201231
- **Application type:** Abbreviated New Drug Application (Generic)
- **Brand name:** DEXMETHYLPHENIDATE HYDROCHLORIDE
- **Generic name:** DEXMETHYLPHENIDATE HYDROCHLORIDE
- **Active ingredients:** DEXMETHYLPHENIDATE HYDROCHLORIDE
- **Dosage form:** TABLET
- **Route:** ORAL
- **Marketing status:** Prescription
- **Sponsor:** SUN PHARM INDUSTRIES
- **Manufacturer:** Sun Pharmaceutical Industries, Inc.
- **First approval:** 2015-09-24
## Source
- [Drugs@FDA application overview](https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=201231)
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