← FDA Drug Approvals (Drugs@FDA)
LEXETTE
NDA · New Drug Application · Sponsor: MAYNE PHARMA · Approved 2018-05-24
Drug application
- FDA Application #
NDA210566
- Application type
- New Drug Application
- Brand name
- LEXETTE
- Generic name
- Halobetasol Propionate
- Active ingredients
- HALOBETASOL PROPIONATE
- Dosage form
- AEROSOL, FOAM
- Route
- TOPICAL
- Marketing status
- Discontinued
- Sponsor
- MAYNE PHARMA
- First approval
- 2018-05-24
Source
- Authoritative
- Drugs@FDA application overview
- Machine
- JSON-LD · Markdown