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
21922-061_e83bff34-44d0-4651-a44f-c4488fb2f3f3
Product NDC
21922-061
Form
SOLUTION
Composition / generic term
clobetasol propionate
Labeler
Encube Ethicals, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20240610
Source listing expiry
20271231

Source-listed ingredients

  • CLOBETASOL PROPIONATE — .5 mg/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BOTTLE in 1 CARTON (21922-061-22) / 25 mL in 1 BOTTLE · 21922-061-22
  • 1 BOTTLE in 1 CARTON (21922-061-27) / 50 mL in 1 BOTTLE · 21922-061-27

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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