Drug recall D-1211-2018
Product
Fenofibrate Tablets, USP 145 mg, 90-count bottles, Rx only, Manufactured for: Camber Pharmaceuticals, Inc. Piscataway, NJ, 08854, NDC 31722-596-90
Reason for recall
Presence of Foreign Tablet/Capsule: A foreign identified as Valacyclovir tablet 500 mg was co-mingled in a bottle containing Fenofibrate Tablets, USP 145 mg.
Lots and codes
Lot #: E181370, Exp. 5/2020
Recall details
- Recalling firm
- Hetero Labs, Ltd. - Unit III, Hyderabad
- Quantity
- 5,424 bottles
- Distribution
- Indiana and Louisiana
- Type
- Voluntary: Firm initiated
- Recall initiated
- September 12, 2018
- Terminated
- November 29, 2018
Related products
- Fenofibrate – drug information
- NDC 31722-595 Fenofibrate · Fenofibrate 48 mg/1 · Camber Pharmaceuticals, Inc.
- NDC 31722-596 Fenofibrate · Fenofibrate 145 mg/1 · Camber Pharmaceuticals, Inc.