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
- 72603-164_adfa045e-ce4b-4195-962f-1c3165667119
- Product NDC
- 72603-164
- Form
- OINTMENT
- Composition / generic term
- Desonide
- Labeler
- NORTHSTAR RX LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230907
- 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 (72603-164-01) / 15 g in 1 TUBE · 72603-164-01
- 1 TUBE in 1 CARTON (72603-164-02) / 60 g in 1 TUBE · 72603-164-02
Source and coverage
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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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