Akron Pharma, Inc. recalls Diphenhydramine HCl 50 mg, 1000 capsules per bottle, Akron Pharma, Manufactured for: Akron Pharma, Inc. 373 Route US 46,
Recalled January 22, 2025 · FDA recall D-0199-2025 · Akron Pharma
Hazard
Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID. · FDA Class III
Units
324 bottles
Sold at
Nationwide in the US
Description
Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Product
Diphenhydramine HCl 50 mg, 1000 capsules per bottle, Akron Pharma, Manufactured for: Akron Pharma, Inc. 373 Route US 46, Building E, Suite 117, Fairfield, NJ 07004, NDC 71399-8026-02.
Manufacturer(s)
Akron Pharma, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →