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FDAFDA · Food and drugs·Recall number D-0098-2024

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.

Published November 15, 2023 · Recall initiated: October 19, 2023

Status when published: Completed — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the hazard

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

What to do

Voluntary: Firm initiated · Letter

Recall details

Brand
OXYBUTYNIN
Manufacturer
Zydus Pharmaceuticals (USA) Inc
Distributor
Nationwide.
Lot
M211541, exp. date 10/2024 M211542, exp. date 10/2024 M212746, exp. date 10/2024 M300660, exp. date 12/2024
Risk classification
Class II
Area (FDA)
drug
Country
United States

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