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
Reported: June 7, 2017 Initiated: April 26, 2017 #D-0868-2017
Product Description
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
Reason for Recall
Subpotent Drug; Clavulanic Acid
Details
- Recalling Firm
- Sandoz Inc
- Units Affected
- 4,464 bottles
- Distribution
- NY, OH
- Location
- Princeton, NJ
Frequently Asked Questions
What product was recalled? ▼
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. Recalled by Sandoz Inc. Units affected: 4,464 bottles.
Why was this product recalled? ▼
Subpotent Drug; Clavulanic Acid
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on June 7, 2017. Severity: Low. Recall number: D-0868-2017.
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