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
- 0472-0380_c08077cb-b3a1-4bd8-85ba-731e73cc66e0
- Product NDC
- 0472-0380
- Form
- CREAM
- Composition / generic term
- Betamethasone Dipropionate
- Labeler
- Actavis Pharma, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20020903
- Source listing expiry
- 20271231
Source-listed ingredients
- BETAMETHASONE DIPROPIONATE — .5 mg/g
These values do not establish equivalence or a dose recommendation.
Packages
- 1 TUBE in 1 CARTON (0472-0380-15) / 15 g in 1 TUBE · 0472-0380-15
- 1 TUBE in 1 CARTON (0472-0380-45) / 45 g in 1 TUBE · 0472-0380-45
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 →