FDA recall record

Teligent Pharma Betamethasone Dipropionate Ointment USP, 0.05% (Augmented) recall — FDA D-0340-2021

Failed Impurities/ Degradation Specifications - OOS for know impurity Betamethasone 17- propionate.

Class IIIclassification
D-0340-2021official record ID
May 5, 2021report date

Recall record at a glance

Official recordD-0340-2021
CategoryDrug Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmTeligent Pharma, Inc.
Report dateMay 5, 2021
Recall initiation dateFeb 2, 2021
QuantityN/A
LocationBuena, NJ, United States

Official product description

Betamethasone Dipropionate Ointment USP, 0.05% (Augmented), packaged in 15 grams tubes, Manufactured by: Teligent Pharma, Inc. Buena, New Jersey 08310, Distributed by: McKesson Corporation dba Sky Packaging 4971 Southbridge Blvd., Suite 101 Memphis, TN 38141, NDC 63739-996-15

Why the product was recalled

Failed Impurities/ Degradation Specifications - OOS for know impurity Betamethasone 17- propionate.

Distribution information

USA 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

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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