United States · FDA National Drug Code directory
Hydrocortisone Butyrate
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
- 68682-271_01f93fa6-5fea-4b3e-aa41-e8e0269257ee
- Product NDC
- 68682-271
- Form
- OINTMENT
- Composition / generic term
- hydrocortisone butyrate
- Labeler
- Oceanside Pharmaceuticals
- Marketing category
- NDA
- Marketing start / end (source format)
- 20090901
- Source listing expiry
- 20261231
Source-listed ingredients
- HYDROCORTISONE BUTYRATE — 1 mg/g
These values do not establish equivalence or a dose recommendation.
Packages
- 1 TUBE in 1 CARTON (68682-271-15) / 15 g in 1 TUBE · 68682-271-15
- 1 TUBE in 1 CARTON (68682-271-45) / 45 g in 1 TUBE · 68682-271-45
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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