NDC 51672-1386
Fluocinonide 0.5 mg per 1 g cream
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
- Mar 25, 2026 · Class II · Sun Pharmaceutical Industries Inc
Failed Viscosity Specifications: Out of Specification results, above the specification limit, in viscosity, noted during stability testing.
Lots: Lot# AD76252, Exp Date: 6/30/2026. - Mar 25, 2026 · Class II · Sun Pharmaceutical Industries Inc
Failed Viscosity Specifications: Out of Specification results, above the specification limit, in viscosity, noted during stability testing.
Lots: Lot# AD76251, Exp Date: 6/30/2026. - Mar 25, 2026 · Class II · Sun Pharmaceutical Industries Inc
Failed Viscosity Specifications: Out of Specification results, above the specification limit, in viscosity, noted during stability testing.
Lots: Lot# AD76250, Exp Date: 6/30/2026.
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Fluocinonide: every company that makes it
- Form
- cream, topical
- Strength
- 0.5 mg per 1 g
- Approval
- ANDA ANDA071500
- On the market since
- Oct 27, 2016
- Package NDCs
51672-1386-151672-1386-251672-1386-351672-1386-4- Official label
- DailyMed (National Library of Medicine), updated Jul 8, 2025
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