FDAFDA · Food and drugs·Recall number D-1211-2018
Fenofibrate Tablets, USP 145 mg, 90-count bottles, Rx only, Manufactured for: Camber Pharmaceuticals, Inc. Piscataway, NJ, 08854, NDC 31722-596-90
Published October 3, 2018 · Recall initiated: September 12, 2018
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
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.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- FENOFIBRATE
- Manufacturer
- Hetero Labs, Ltd. - Unit III
- Distributor
- Indiana and Louisiana
- UPC
- 0331722596305
- Lot
- Lot #: E181370, Exp. 5/2020
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- India
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