← FDA Drug Approvals (Drugs@FDA)
OLUX E
NDA · New Drug Application · Sponsor: PHARMOBEDIENT · Approved 2007-01-12
Drug application
- FDA Application #
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
- Authoritative
- Drugs@FDA application overview
- Machine
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