RecallRadar

FDA Drug recall D-0996-2019

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

On 2019-03-20 the FDA classified a Class III recall of Oxybutynin Chloride, Extended-Release Tablets USP, 10 mg, 100 Tablet, Rx Only, Distributed by: Lannett Company, Inc, Philadelphia, PA 19154… by Lannett, citing failed Dissolution Specifications.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0996-2019
ClassificationClass III
Statusterminated
Initiated2019-02-21
Published2019-03-20
Last updated2026-09-13 11:52 UTC
CompanyLannett
DistributionUS

Product

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

Reason

Failed Dissolution Specifications

Identifiers

ndc62175-270-37
ndc62175-270-41
ndc62175-271-37
ndc62175-271-41
ndc62175-272-37
ndc62175-272-41
code_infoLots: 18226783A, exp 07/2021 and 18232540A, exp 08/2021

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0996-2019%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.