Drug recall D-1836-2019
Product
Bexarotene Capsules, 75 mg, 100 capsules per bottle, Rx Only, Manufactured for: Upsher-Smith Laboratories, LLC, Maple Grove, MN 55369. NDC: 0832-0285-00
Reason for recall
Failed Dissolution Specifications
Lots and codes
Lot: A2610. exp 3/2020
Recall details
- Recalling firm
- Upsher Smith Laboratories, Inc., Maple Grove, MN
- Quantity
- 166 bottles
- Distribution
- KY, OH, NJ, LA
- Type
- Voluntary: Firm initiated
- Recall initiated
- July 29, 2019
- Terminated
- August 25, 2022
Related products
- Bexarotene – drug information
- NDC 0832-0285 Bexarotene · Bexarotene 75 mg/1 · Upsher-Smith Laboratories, Inc.