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Akorn, Inc. recalls Olopatadine HCl Nasal Spray, 665 mcg, 30.5 g bottles, Rx Only, Manufactured by: Akorn, Operating Company LLC, Gurnee, IL

Recalled June 7, 2023 · FDA recall D-0832-2023 · Akorn

Hazard
CGMP Deviations: Firm went out of business and could no longer continue stability studies. · FDA Class II
Units
N/A
Sold at
Nationwide in the USA and Puerto Rico

Description

CGMP Deviations: Firm went out of business and could no longer continue stability studies.

Product
Olopatadine HCl Nasal Spray, 665 mcg, 30.5 g bottles, Rx Only, Manufactured by: Akorn, Operating Company LLC, Gurnee, IL 60031. ALL NDCs
Manufacturer(s)
Akorn, Inc.

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov

Akorn, Inc. recalls Olopatadine HCl Nasal Spray, 665 mcg, 30.5 g bottles, Rx Only, Manufactured by: Akorn, Operating Company LLC, Gurnee, IL | RecallWatchUSA