Sandoz Inc recalls Amoxicillin and Clavulanate Potassium Tablets, USP, 500 mg/125 mg, in 20 count bottles, Rx Only, Manufactured in Austri…

Recall date

April 26, 2017

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

D-0868-2017

FDA classification

Class III

Brand / firm

Sandoz Inc

Sold / distributed

NY, OH

Why it was recalled

Subpotent Drug; Clavulanic Acid

Class III means the product violates regulations but is not likely to cause harm.

What 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