OLUX
- Product NDC
- 40076-031
- 11-digit product format
- 400760031
- Labeler code
- 40076
- Product ID
- 40076-031_78aa8bef-d16f-4326-9cff-b30a7b427aa1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- clobetasol propionate
- Dosage form
- AEROSOL, FOAM
- Route
- TOPICAL
- Labeler
- Prestium Pharma, Inc.
- Application
- NDA021142
- Marketing category
- NDA
- Marketing start
- 2014-02-07
- Marketing end
- 2020-02-29
- Substance
- CLOBETASOL PROPIONATE
- Active strength
- 1 mg/g
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record