# MEMANTINE HYDROCHLORIDE
> **ANDA205905** · Abbreviated New Drug Application (Generic) · Sponsor: SUN PHARM · Approved 2016-09-28
## Drug
- **FDA Application Number:** ANDA205905
- **Application type:** Abbreviated New Drug Application (Generic)
- **Brand name:** MEMANTINE HYDROCHLORIDE
- **Generic name:** Memantine Hydrochloride
- **Active ingredients:** MEMANTINE HYDROCHLORIDE
- **Dosage form:** CAPSULE, EXTENDED RELEASE
- **Route:** ORAL
- **Marketing status:** Discontinued
- **Sponsor:** SUN PHARM
- **First approval:** 2016-09-28
## Source
- [Drugs@FDA application overview](https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=205905)
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