# ORUDIS
> **NDA018754** · New Drug Application · Sponsor: WYETH AYERST · Approved 1986-01-09
## Drug
- **FDA Application Number:** NDA018754
- **Application type:** New Drug Application
- **Brand name:** ORUDIS
- **Generic name:** Ketoprofen
- **Active ingredients:** KETOPROFEN
- **Dosage form:** CAPSULE
- **Route:** ORAL
- **Marketing status:** Discontinued
- **Sponsor:** WYETH AYERST
- **First approval:** 1986-01-09
## Source
- [Drugs@FDA application overview](https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=018754)
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