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
- 51672-4074_569a2af8-f939-4967-e063-6394a90a7726
- Product NDC
- 51672-4074
- Form
- CREAM
- Composition / generic term
- Hydrocortisone Butyrate
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20050804
- Source listing expiry
- 20271231
Source-listed ingredients
- HYDROCORTISONE BUTYRATE — 1 mg/g
These values do not establish equivalence or a dose recommendation.
Packages
- 1 TUBE in 1 CARTON (51672-4074-1) / 15 g in 1 TUBE · 51672-4074-1
- 1 TUBE in 1 CARTON (51672-4074-2) / 30 g in 1 TUBE · 51672-4074-2
- 5 g in 1 TUBE (51672-4074-5) · 51672-4074-5
- 1 TUBE in 1 CARTON (51672-4074-6) / 45 g in 1 TUBE · 51672-4074-6
- 1 TUBE in 1 CARTON (51672-4074-7) / 10 g in 1 TUBE · 51672-4074-7
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 →