# OXYCODONE HYDROCHLORIDE AND IBUPROFEN
> **ANDA078394** · Abbreviated New Drug Application (Generic) · Sponsor: WATSON LABS · Approved 2007-11-26
## Drug
- **FDA Application Number:** ANDA078394
- **Application type:** Abbreviated New Drug Application (Generic)
- **Brand name:** OXYCODONE HYDROCHLORIDE AND IBUPROFEN
- **Generic name:** Ibuprofen
- **Active ingredients:** IBUPROFEN; OXYCODONE HYDROCHLORIDE
- **Dosage form:** TABLET
- **Route:** ORAL
- **Marketing status:** Discontinued
- **Sponsor:** WATSON LABS
- **First approval:** 2007-11-26
## Source
- [Drugs@FDA application overview](https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=078394)
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