LEXETTE .5 mg/g
halobetasol propionate · AEROSOL, FOAM · Mayne Pharma
No Recall History
Plain English
LEXETTE is a aerosol, foam containing halobetasol propionate at .5 mg/g, taken topical. Manufactured by Mayne Pharma.
Key Facts
- Brand Name
- LEXETTE
- Generic Name
- halobetasol propionate
- NDC Code (Product)
51862-618- Manufacturer
- Mayne Pharma
- Strength
- .5 mg/g
- Dosage Form
- AEROSOL, FOAM
- Route
- TOPICAL
- Marketing Status
- Application #
- ANDA215266
- Marketing Start
- 08/08/2025
Recall History
No Recall HistoryFrequently Asked Questions
What is LEXETTE used for?
LEXETTE contains halobetasol propionate. It is a aerosol, foam taken topical. Consult your doctor for specific uses.
Is LEXETTE a controlled substance?
LEXETTE is not classified as a controlled substance by the DEA.
What is the generic name for LEXETTE?
The generic name for LEXETTE is halobetasol propionate. There are 12 other brand versions of halobetasol propionate.
What is the NDC code for LEXETTE .5 mg/g?
The NDC (National Drug Code) for LEXETTE .5 mg/g is 51862-618, listed by Mayne Pharma.
Other Halobetasol Brands
See all →- Halobetasol Propionate.5 mg/g72162-2067
- Duobrii.1 mg/g0187-0653
- Halobetasol Propionate.5 mg/g70752-119
- Halobetasol Propionate.5 mg/g0713-0339
- Halobetasol Propionate.5 mg/g0713-0640
- Halobetasol Propionate.5 mg/g85437-008
- Bryhali.1 mg/g0187-0002
- Halobetasol Propionate.5 mg/g45802-131
- Halobetasol Propionate.5 mg/g63629-8665
- Halobetasol propionate.5 mg/g68308-769
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)