United States · FDA National Drug Code directory

Desonide

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
80425-0418_1d76541f-80d7-2a55-e063-6294a90aa5f9
Product NDC
80425-0418
Form
CREAM
Composition / generic term
Desonide
Labeler
Advanced Rx of Tennessee, LLC
Marketing category
ANDA
Marketing start / end (source format)
20240717
Source listing expiry
20261231

Source-listed ingredients

  • DESONIDE — .5 mg/g

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 TUBE in 1 CARTON (80425-0418-1) / 60 g in 1 TUBE · 80425-0418-1

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.

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