US Drug Recall Register
Class I · High risk Terminated Initiated Mar 8, 2022 (4 years ago)

Meclizine Hydrochloride Tablets USP, 12.5 mg, packaged in a case of 24 bottles (100-count…

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Labeling: Label mix-up: Incorrect label placed on product. Shipper cases labeled Meclizine Hydrochloride Tablets contain bottles incorrectly labeled as PredniSONE Tablets. The tablets in the bottles are Meclizine Hydrochloride

What was recalled

Meclizine Hydrochloride Tablets USP, 12.5 mg, packaged in a case of 24 bottles (100-count bottle), Rx only, Manufactured by: Jubilant Cadista Pharmaceuticals, Inc., Salisbury, MD, 21801, NDC 59746-122-06

Recalling firm
Jubilant Cadista Pharmaceuticals, Inc.
NDC code
59746-122-06
Origin
MD, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0767-2022

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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