US Drug Recall Register
Class II · Moderate risk Terminated Initiated Dec 2, 2019 (7 years ago)

Amantadine Hydrochloride Tablets, 100 mg, 100-count bottle, Rx only, Manufactured by…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Presence of Foreign Substance: Presence of a foreign object in a single tablet.

What was recalled

Amantadine Hydrochloride Tablets, 100 mg, 100-count bottle, Rx only, Manufactured by: Jubilant Generics Ltd., Roorkee-247661, India; Marketed by: Jubilant Cadista Pharmaceuticals Inc., Salisbury, MD 21801, USA; NDC 59746-699-01.

Recalling firm
Jubilant Cadista Pharmaceuticals, Inc.
NDC code
59746-699-01
Origin
MD, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0576-2020

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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