US Drug Recall Register
Class III · Low risk Terminated Initiated Dec 13, 2016 (10 years ago)

Donepezil Hydrochloride Tablets, 10 mg, packaged in a) 30-count bottles (NDC…

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Subpotent Drug: out of specification results for assay test.

What was recalled

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.

Recalling firm
Sandoz Inc
NDC code
0781-5275-31
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0435-2017

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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