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
- 50090-7517_3140f140-758c-41a6-83e2-8cb9be901863
- Product NDC
- 50090-7517
- Form
- OINTMENT, AUGMENTED
- Composition / generic term
- betamethasone dipropionate
- Labeler
- A-S Medication Solutions
- Marketing category
- ANDA
- Marketing start / end (source format)
- 19990622
- Source listing expiry
- 20261231
Source-listed ingredients
- BETAMETHASONE DIPROPIONATE — .5 mg/g
These values do not establish equivalence or a dose recommendation.
Packages
- 50 g in 1 TUBE (50090-7517-0) · 50090-7517-0
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 →