United States · FDA National Drug Code directory

LEXETTE

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
51862-618_8aa1f819-c81f-4af1-aaa7-353df3203ff6
Product NDC
51862-618
Form
AEROSOL, FOAM
Composition / generic term
halobetasol propionate
Labeler
Mayne Pharma
Marketing category
ANDA
Marketing start / end (source format)
20250808
Source listing expiry
20261231

Source-listed ingredients

  • HALOBETASOL PROPIONATE — .5 mg/g

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 CANISTER in 1 CARTON (51862-618-50) / 50 g in 1 CANISTER · 51862-618-50

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

Browse United States records →