Drug recall D-0275-2024
Product
Budesonide Extended-Release Tablets 9mg, 30-count bottle, Rx Only, Manufactured by: Actavis Laboratories FL, Inc., Fort Lauderdale, FL 33314 USA, Distributed by: Actavis Pharma, Inc., Parsippany, NJ 07054 USA, NDC 0591-2510-30
Reason for recall
Failed Dissolution Specifications
Lots and codes
Lot # 100047273; Exp. 07/2025
Recall details
- Recalling firm
- Teva Pharmaceuticals USA, Inc, Parsippany, NJ
- Quantity
- 10,672 30-count bottles
- Distribution
- Nationwide
- Type
- Voluntary: Firm initiated
- Recall initiated
- January 8, 2024
Related products
- budesonide – drug information
- NDC 0591-2510 Budesonide · Budesonide 9 mg/1 · Actavis Pharma, Inc.