FDA recall record

Sandoz Donepezil Hydrochloride Tablets, 10 mg recall — FDA D-0435-2017

Subpotent Drug: out of specification results for assay test.

Class IIIclassification
D-0435-2017official record ID
Jan 25, 2017report date

Recall record at a glance

Official recordD-0435-2017
CategoryDrug Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmSandoz Inc.
Report dateJan 25, 2017
Recall initiation dateDec 13, 2016
Quantitya) 10,200 bottles; b) 300 bottles
LocationPrinceton, NJ, United States

Official product description

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.

Why the product was recalled

Subpotent Drug: out of specification results for assay test.

Distribution information

Nationwide in the USA

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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