FDAFDA · Food and drugs·Recall number D-66373-001
Hydroxychloroquine Sulfate Tablets, USP, 200 mg, Rx Only, 100 Tablets per bottle, Sandoz Inc., Princeton NJ, 08540, NDC 0781-1407-01.
Published October 16, 2013 · Recall initiated: September 25, 2013
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
Failed Tablet/Capsule Specifications: Sandoz is recalling one lot of Hydroxychloroquine Sulfate Tablets, USP, 200mg, due to illegibility of the logo on some tablets.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Sandoz Incorporated
- Distributor
- Nationwide
- Lot
- Lot #: BU3417, Exp 06/2014
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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