FDAFDA · Food and drugs·Recall number D-0868-2017
Amoxicillin and Clavulanate Potassium Tablets, USP, 500 mg/125 mg, in 20 count bottles, Rx Only, Manufactured in Austria by Sandoz Gmbh for Sandoz Inc. Princeton NJ NDC 0781-1831-20
Published June 7, 2017 · Recall initiated: April 26, 2017
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
Subpotent Drug; Clavulanic Acid
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- AMOXICILLIN AND CLAVULANATE POTASSIUM
- Manufacturer
- Sandoz Inc
- Distributor
- NY, OH
- UPC
- 0307816102462
- Lot
- Lot FP8735, 8/2017
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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