Drug recall D-0611-2026
Product
Fenofibrate Capsules, USP 200 mg, Rx only, 100 Capsules, Manufactured by: Ajanta Pharma Limited, India, Marketed by: Ajanta Pharma USA Inc. Bridgewater, NJ 08807, NDC 27241-120-04.
Reason for recall
CGMP Deviations
Lots and codes
Lot # PA02216; Exp. 12/2029
Recall details
- Recalling firm
- Ajanta Pharma USA Inc, Bridgewater, NJ
- Quantity
- 3648 bottles
- Distribution
- U.S. Nationwide
- Type
- Voluntary: Firm initiated
- Recall initiated
- May 28, 2026
Related products
- Fenofibrate – drug information
- NDC 27241-119 Fenofibrate · Fenofibrate 134 mg/1 · Ajanta Pharma USA Inc.
- NDC 27241-118 Fenofibrate · Fenofibrate 67 mg/1 · Ajanta Pharma USA Inc.
- NDC 27241-120 Fenofibrate · Fenofibrate 200 mg/1 · Ajanta Pharma USA Inc.