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
- 35573-107_c8bda9a8-4dec-4084-84e5-4b4623390bd8
- Product NDC
- 35573-107
- Form
- OINTMENT, AUGMENTED
- Composition / generic term
- BETAMETHASONE DIPROPIONATE
- Labeler
- Burel Pharmaceuticals, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250115
- Source listing expiry
- 20261231
Source-listed ingredients
- BETAMETHASONE DIPROPIONATE — .5 mg/g
These values do not establish equivalence or a dose recommendation.
Packages
- 1 TUBE in 1 CARTON (35573-107-15) / 15 g in 1 TUBE · 35573-107-15
- 1 TUBE in 1 CARTON (35573-107-49) / 50 g in 1 TUBE · 35573-107-49
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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