# OLUX E
> **NDA022013** · New Drug Application · Sponsor: PHARMOBEDIENT · Approved 2007-01-12
## Drug
- **FDA Application Number:** NDA022013
- **Application type:** New Drug Application
- **Brand name:** OLUX E
- **Generic name:** Clobetasol Propionate
- **Active ingredients:** CLOBETASOL PROPIONATE
- **Dosage form:** AEROSOL, FOAM
- **Route:** TOPICAL
- **Marketing status:** Discontinued
- **Sponsor:** PHARMOBEDIENT
- **First approval:** 2007-01-12
## Source
- [Drugs@FDA application overview](https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=022013)
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