United States · FDA National Drug Code directory
CLOBETASOL PROPIONATE
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
- 59651-732_51e53193-523e-4367-a405-8ab44df55358
- Product NDC
- 59651-732
- Form
- OINTMENT
- Composition / generic term
- CLOBETASOL PROPIONATE
- Labeler
- Aurobindo Pharma Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230928
- Source listing expiry
- 20261231
Source-listed ingredients
- CLOBETASOL PROPIONATE — .5 mg/g
These values do not establish equivalence or a dose recommendation.
Packages
- 1 TUBE in 1 CARTON (59651-732-14) / 15 g in 1 TUBE · 59651-732-14
- 1 TUBE in 1 CARTON (59651-732-30) / 30 g in 1 TUBE · 59651-732-30
- 1 TUBE in 1 CARTON (59651-732-46) / 45 g in 1 TUBE · 59651-732-46
- 1 TUBE in 1 CARTON (59651-732-60) / 60 g in 1 TUBE · 59651-732-60
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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