FDAFebruary 21, 2019drug

Oxybutynin Chloride, Extended-Release Tablets USP, 10 mg, 100 Tablet, Rx Only, Distributed by: Lannett Company, Inc, Philadelphia, PA 19154 NDC: 62175-271-37

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Failed Dissolution Specifications

What to do

FDA enforcement status: Terminated

Brands named

lannett

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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Oxybutynin Chloride, Extended-Release Tablets USP, 10 mg, 100 Tablet, Rx Only, Distributed by: Lannett Company, Inc, Philadelphia, PA 19154 NDC: 62175-271-37 — Recall Details · AllClear