US Drug Recall Register
Class II · Moderate risk Terminated Initiated Mar 8, 2012 (14 years ago)

Nisoldipine Extended Release Tablets, 17mg, 100 count bottle, Rx only, Manufactured for…

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

Why it was recalled

Failed USP Dissolution Test Requirements: Out of Specification dissolution result at 18 month time point

What was recalled

Nisoldipine Extended Release Tablets, 17mg, 100 count bottle, Rx only, Manufactured for: Prasco Laboratories Mason OH 45040, Manufactured by SkyePharma production SAS 38297, Saint Quentin-Pallavier, France, NDC: 0677-1979-01

Recalling firm
Shionogi Inc.
Origin
GA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1398-2012

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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