NDC 51672-1264 – Fluocinonide
Fluocinonide .5 mg/g · Ointment · Topical
Product NDC51672-1264
Product details
- Brand name
- Fluocinonide
- Generic name
- Fluocinonide
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Ointment
- Route
- Topical
- Marketing category
- ANDA · ANDA075008
- Marketed since
- June 30, 1999
- Listing expires
- December 31, 2026
- Pharmacologic class
- Corticosteroid
Active ingredients
- Fluocinonide .5 mg/g
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 51672-1264-1 | 1 TUBE in 1 CARTON (51672-1264-1) / 15 g in 1 TUBE | Jun 30, 1999 |
| 51672-1264-2 | 1 TUBE in 1 CARTON (51672-1264-2) / 30 g in 1 TUBE | Jun 30, 1999 |
| 51672-1264-3 | 1 TUBE in 1 CARTON (51672-1264-3) / 60 g in 1 TUBE | Jun 30, 1999 |
Recalls mentioning this NDC
- D-0146-2018 Nov 1, 2017 · Class III
Cross contamination with other products: traces of Dapsone were found in the finished product. - D-0790-2017 May 24, 2017 · Class III
Cross contamination with other products: Certain lots of Fluocinonide Cream were found to be contaminated with a small quantity of hydrocortisone-17-valerate.
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- 63629-2508 Fluocinonide 1 mg/g · Cream · Bryant Ranch Prepack