PlainRecalls
FDA Drug Moderate Class II Terminated

Betamethasone Dipropionate Lotion USP, 0.05% (Augmented), 30 mL bottle, (29 g), Rx Only, Teligent Pharma Inc., Buena, NJ, 08310, NDC 52565-023-29

Reported: January 5, 2022 Initiated: August 23, 2021 #D-0297-2022

Product Description

Betamethasone Dipropionate Lotion USP, 0.05% (Augmented), 30 mL bottle, (29 g), Rx Only, Teligent Pharma Inc., Buena, NJ, 08310, NDC 52565-023-29

Reason for Recall

Failed Stability Specifications: lot did not meet specification for the Active Pharmaceutical Ingredient (API) particle test, which was determined through routine stability testing

Details

Recalling Firm
Teligent Pharma, Inc.
Units Affected
3,792 bottles
Distribution
Distributed Nationwide in the USA
Location
Buena, NJ

Frequently Asked Questions

What product was recalled?
Betamethasone Dipropionate Lotion USP, 0.05% (Augmented), 30 mL bottle, (29 g), Rx Only, Teligent Pharma Inc., Buena, NJ, 08310, NDC 52565-023-29. Recalled by Teligent Pharma, Inc.. Units affected: 3,792 bottles.
Why was this product recalled?
Failed Stability Specifications: lot did not meet specification for the Active Pharmaceutical Ingredient (API) particle test, which was determined through routine stability testing
Which agency issued this recall?
This recall was issued by the FDA Drug on January 5, 2022. Severity: Moderate. Recall number: D-0297-2022.