FDA recall record

Teligent Pharma Fluocinonide Ointment USP 0.05% recall — FDA D-0064-2021

Failed Impurities/Degradation - Out-of-specification results for Fluocinolone Acetonide impurity.

Class IIIclassification
D-0064-2021official record ID
Nov 11, 2020report date

Recall record at a glance

Official recordD-0064-2021
CategoryDrug Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmTeligent Pharma, Inc.
Report dateNov 11, 2020
Recall initiation dateSep 28, 2020
Quantity36,790 tubes
LocationBuena, NJ, United States

Official product description

Fluocinonide Ointment USP 0.05%, packaged in: a) 15 gm tube, NDC 52565-0040-15, b) 30 gm tube, NDC 52565-0040-30 c) 60 gram tube, NDC 52565-0040-60, Rx only, Manufactured by: Teligent Pharma, Inc., Buena, New Jersey 08310

Why the product was recalled

Failed Impurities/Degradation - Out-of-specification results for Fluocinolone Acetonide impurity.

Distribution information

United States Nationwide

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

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About this record

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