Betamethasone Dipropionate Lotion USP, 0.05%* (Augmented), packaged in a) 30 mL (29 grams) bottles, NDC 52565-023-29; b) 60 mL (58 grams) bottles, NDC 52565-023-59, Rx Only, Teligent Pharma, Inc., Buena, NJ 08310
Reported: March 30, 2022 Initiated: March 15, 2022 #D-0669-2022
Product Description
Betamethasone Dipropionate Lotion USP, 0.05%* (Augmented), packaged in a) 30 mL (29 grams) bottles, NDC 52565-023-29; b) 60 mL (58 grams) bottles, NDC 52565-023-59, Rx Only, Teligent Pharma, Inc., Buena, NJ 08310
Reason for Recall
cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.
Details
- Recalling Firm
- Teligent Pharma, Inc.
- Units Affected
- 43,218 bottles
- Distribution
- Nationwide in the USA and Puerto Rico
- Location
- Buena, NJ
Frequently Asked Questions
What product was recalled? ▼
Betamethasone Dipropionate Lotion USP, 0.05%* (Augmented), packaged in a) 30 mL (29 grams) bottles, NDC 52565-023-29; b) 60 mL (58 grams) bottles, NDC 52565-023-59, Rx Only, Teligent Pharma, Inc., Buena, NJ 08310. Recalled by Teligent Pharma, Inc.. Units affected: 43,218 bottles.
Why was this product recalled? ▼
cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on March 30, 2022. Severity: Moderate. Recall number: D-0669-2022.
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