# XARTEMIS XR
> **NDA204031** · New Drug Application · Sponsor: MALLINCKRODT INC · Approved 2014-03-11
## Drug
- **FDA Application Number:** NDA204031
- **Application type:** New Drug Application
- **Brand name:** XARTEMIS XR
- **Generic name:** Acetaminophen
- **Active ingredients:** ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
- **Dosage form:** TABLET, EXTENDED RELEASE
- **Route:** ORAL
- **Marketing status:** Discontinued
- **Sponsor:** MALLINCKRODT INC
- **First approval:** 2014-03-11
## Source
- [Drugs@FDA application overview](https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=204031)
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