US Drug Recall Register
Class II · Moderate risk Completed Initiated Oct 19, 2023 (3 years ago)

Oxybutynin Chloride Extended-Release Tablet USP, 15 mg, 100 count bottles, Rx Only…

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

Why it was recalled

Failed Dissolution Specifications-out-of-specification (OOS) test results observed for dissolution at the 6 month long term time point.

What was recalled

Oxybutynin Chloride Extended-Release Tablet USP, 15 mg, 100 count bottles, Rx Only, Manufactured by: Cadila Healthcare Ltd, Baddi, India. Distributed by: Zydus Pharmaceuticals (USA) Inc. NDC # 68382-257-01.

Recalling firm
Zydus Pharmaceuticals (USA) Inc
NDC code
68382-257-01
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0098-2024

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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