NDC 51672-1261
Desoximetasone 0.5 mg per 1 g gel
On the label: Caraco Pharmaceutical Laboratories, Ltd..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Sun Pharma Canada Inc. | Brampton, Canada | Makes it | No problems foundMar 27, 2026 · 7 inspections |
Recalls
- Sep 13, 2016 · Class II · Taro Pharmaceuticals, Inc.
Failed Stability Specifications: The subject lots exhibited OOS results for Homogeneity test (Moderate separation).
Lots: Lot #: B5093-18608, B5094-18608, Exp. Jan 2017; Lot #: C5141-18954, C5142-18954, E5109-19625, Exp . Feb 2017 - Sep 13, 2016 · Class II · Taro Pharmaceuticals, Inc.
Failed Stability Specifications: The subject lots exhibited OOS results for Homogeneity test (Moderate separation).
Lots: Lot #: E0598-19624, E5099-19624, Exp. Jan 2017
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Desoximetasone: every company that makes it
- Form
- gel, topical
- Strength
- 0.5 mg per 1 g
- Approval
- ANDA ANDA074904
- On the market since
- Jul 14, 1998
- Package NDCs
51672-1261-151672-1261-251672-1261-3- Official label
- DailyMed (National Library of Medicine), updated Jul 2, 2025
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