US Drug Recall Register
Class II · Moderate risk Terminated Initiated May 30, 2023 (3 years ago)

Extended Phenytoin Sodium Capsules, USP, 100 mg, Rx Only, 100 capsules per bottle…

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

Why it was recalled

Failed Dissolution Specifications: Out-of-specification results for dissolution (above specification)

What was recalled

Extended Phenytoin Sodium Capsules, USP, 100 mg, Rx Only, 100 capsules per bottle, Distributed by: Amneal Pharmaceuticals LLC., Bridgewater, NJ 08807, NDC 65162-212-10.

Recalling firm
Amneal Pharmaceuticals of New York, LLC
NDC code
65162-212-10
Origin
NY, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0876-2023

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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