United States · FDA National Drug Code directory
Betamethasone Dipropionate
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
- 21922-104_cb91d996-4591-4ff4-8468-186aa4f7d837
- Product NDC
- 21922-104
- Form
- LOTION, AUGMENTED
- Composition / generic term
- BETAMETHASONE DIPROPIONATE
- Labeler
- Encube Ethicals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20251125
- Source listing expiry
- 20261231
Source-listed ingredients
- BETAMETHASONE DIPROPIONATE — .5 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE, PLASTIC in 1 CARTON (21922-104-01) / 60 mL in 1 BOTTLE, PLASTIC · 21922-104-01
- 1 BOTTLE, PLASTIC in 1 CARTON (21922-104-21) / 30 mL in 1 BOTTLE, PLASTIC · 21922-104-21
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 →