NDC 68788-8554
Fluocinonide 0.5 mg per 1 g ointment
On the label: Preferred Pharmaceuticals, Inc... It's repackaged: Preferred Pharmaceuticals, Inc.. rebottles it from Caraco Pharmaceutical Laboratories, Ltd.'s NDC 51672-1264.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Sun Pharma Canada Inc. | Brampton, Canada | Makes it | No problems foundMar 27, 2026 · 7 inspections |
Repackaging site
- Preferred Pharmaceuticals Inc., Anaheim, CA, United States · relabels it
Recalls
- Sep 20, 2017 · Class III · Taro Pharmaceuticals U.S.A., Inc.
Cross contamination with other products: traces of Dapsone were found in the finished product.
Lots: Lot #: A771026850, Exp 6/18 - Mar 17, 2017 · Class III · Taro Pharmaceuticals U.S.A., Inc.
Cross contamination with other products: Certain lots of Fluocinonide Cream were found to be contaminated with a small quantity of hydrocortisone-17-valerate.
Lots: Lot #: D301311473, D301411473, Exp 3/2017
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Fluocinonide: every company that makes it
- Form
- ointment, topical
- Strength
- 0.5 mg per 1 g
- Approval
- ANDA ANDA075008
- On the market since
- Nov 20, 2023
- Package NDCs
68788-8554-6- Official label
- DailyMed (National Library of Medicine), updated Apr 17, 2026
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