US Drug Recall Register
Class II · Moderate risk Terminated Initiated Sep 26, 2014 (12 years ago)

Venlafaxine Hydrochloride Extended-Release Tablets, 37.5 mg, 30-count bottles and…

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

Why it was recalled

Failed Dissolution Specifications; 12 month stability time point

What was recalled

Venlafaxine Hydrochloride Extended-Release Tablets, 37.5 mg, 30-count bottles and 90-count bottles, RX only, Manufactured for Sun Pharma Global Inc. Dubai, United Arab Emirates by Sun Pharmaceutical Industries Limited, Halol, India

Recalling firm
Sun Pharma Global Inc.
Origin
N/A, United Arab Emirates
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0236-2015

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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