US Drug Recall Register
Class II · Moderate risk Terminated Initiated Sep 16, 2022 (4 years ago)

Neoral soft gelatin capsules (cyclosporine capsules, USP) Modified, 25 mg, Rx Only, 30…

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

Why it was recalled

CGMP deviations: Out of specification results obtained during routine stability testing for ethanol content.

What was recalled

Neoral soft gelatin capsules (cyclosporine capsules, USP) Modified, 25 mg, Rx Only, 30 Soft Gelatin Capsules per carton, Mfg by: Novartis Pharmaceuticals Corporation, East Hanover, NJ 07936, NDC # 0078-0246-15.

Recalling firm
Novartis Pharmaceuticals Corporation
NDC code
0078-0246-15
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1543-2022

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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