Sandoz Inc recalls Donepezil Hydrochloride Tablets, 10 mg, packaged in a) 30-count bottles (NDC 0781-5275-31) and b) 1000-count bottles (ND
Recalled January 25, 2017 · FDA recall D-0435-2017 · Sandoz
Hazard
Subpotent Drug: out of specification results for assay test. · FDA Class III
Units
a) 10,200 bottles; b) 300 bottles
Sold at
Nationwide in the USA
Description
Subpotent Drug: out of specification results for assay test.
Product
Donepezil Hydrochloride Tablets, 10 mg, packaged in a) 30-count bottles (NDC 0781-5275-31) and b) 1000-count bottles (NDC 0781-5275-10), Rx only, Manufactured in India by Sandoz Private Ltd for Sandoz Inc., Princeton, NJ 08540.
Manufacturer(s)
Sandoz Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →