# PAROXETINE HYDROCHLORIDE
> **ANDA213612** · Abbreviated New Drug Application (Generic) · Sponsor: EPIC PHARMA LLC · Approved 2021-08-11
## Drug
- **FDA Application Number:** ANDA213612
- **Application type:** Abbreviated New Drug Application (Generic)
- **Brand name:** PAROXETINE HYDROCHLORIDE
- **Generic name:** Paroxetine Hydrochloride
- **Active ingredients:** PAROXETINE HYDROCHLORIDE
- **Dosage form:** TABLET, EXTENDED RELEASE
- **Route:** ORAL
- **Marketing status:** Discontinued
- **Sponsor:** EPIC PHARMA LLC
- **First approval:** 2021-08-11
## Source
- [Drugs@FDA application overview](https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=213612)
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*MORVS · CC0 1.0*