Fenofibrate Tablets, USP 145 mg, 90-count bottles, Rx only, Manufactured for: Camber Pharmaceuticals, Inc. Piscataway, NJ, 08854, NDC 31722-596-90
Reported: October 3, 2018 Initiated: September 12, 2018 #D-1211-2018
Product Description
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.
Details
- Recalling Firm
- Hetero Labs, Ltd. - Unit III
- Units Affected
- 5,424 bottles
- Distribution
- Indiana and Louisiana
- Location
- Hyderabad
Frequently Asked Questions
What product was recalled? ▼
Fenofibrate Tablets, USP 145 mg, 90-count bottles, Rx only, Manufactured for: Camber Pharmaceuticals, Inc. Piscataway, NJ, 08854, NDC 31722-596-90. Recalled by Hetero Labs, Ltd. - Unit III. Units affected: 5,424 bottles.
Why was this product recalled? ▼
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.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on October 3, 2018. Severity: Low. Recall number: D-1211-2018.
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