Betamethasone Dipropionate Ointment USP, 0.05%* (Augmented), a) 15 gram (NDC 52565-019-15) and b) 50 gram (NDC 52565-019-51) tubed, Rx Only, Manufactured by: Teligent Pharma, Inc. Buena, New Jersey 06310
Reported: June 26, 2019 Initiated: May 20, 2019 #D-1391-2019
Product Description
Betamethasone Dipropionate Ointment USP, 0.05%* (Augmented), a) 15 gram (NDC 52565-019-15) and b) 50 gram (NDC 52565-019-51) tubed, Rx Only, Manufactured by: Teligent Pharma, Inc. Buena, New Jersey 06310
Reason for Recall
Failed Impurities/Degradation Specifications
Details
- Recalling Firm
- Teligent Pharma, Inc.
- Units Affected
- 9360 tubes
- Distribution
- Nationwide
- Location
- Buena, NJ
Frequently Asked Questions
What product was recalled? ▼
Betamethasone Dipropionate Ointment USP, 0.05%* (Augmented), a) 15 gram (NDC 52565-019-15) and b) 50 gram (NDC 52565-019-51) tubed, Rx Only, Manufactured by: Teligent Pharma, Inc. Buena, New Jersey 06310. Recalled by Teligent Pharma, Inc.. Units affected: 9360 tubes.
Why was this product recalled? ▼
Failed Impurities/Degradation Specifications
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on June 26, 2019. Severity: Low. Recall number: D-1391-2019.
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