US Drug Recall Register
Class III · Low risk Terminated Initiated Aug 20, 2021 (5 years ago)

Donepezil HCL Tablets, USP, 5 mg, 90-count bottle, Rx only, Manufactured by: Jubilant…

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

Why it was recalled

Subpotent

What was recalled

Donepezil HCL Tablets, USP, 5 mg, 90-count bottle, Rx only, Manufactured by: Jubilant Generics Ltd. India, Marketed by: Jubilant Cadista Pharmaceuticals Inc. Salisbury, MD 21801 NDC 59746-329-90

Recalling firm
Jubilant Cadista Pharmaceuticals, Inc.
NDC code
59746-329-90
Origin
MD, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0784-2021

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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