US Drug Recall Register
Class II · Moderate risk Terminated Initiated Mar 5, 2013 (14 years ago)

Venlafaxine Hydrochloride Tablets, 75 mg*, 100-count tablets per bottle, Rx only…

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

Why it was recalled

Failed Tablet/Capsule Specifications: Pharmacist complaint of an excessive amount of broken and/or chipped tablets in the bottle.

What was recalled

Venlafaxine Hydrochloride Tablets, 75 mg*, 100-count tablets per bottle, Rx only, Manufactured by: Cadila Healthcare Ltd., Ahmedabad, India; Distributed by: Zydus Pharmaceuticals USA Inc., Pennington, NJ 08534, NDC 68382-021-01.

Recalling firm
Zydus Pharmaceuticals USA Inc
NDC code
68382-021-01
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-202-2013

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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