D-0552-2023 Class II Ongoing

Recalled by Northwind Pharmaceuticals LLC — Indianapolis, IN

Recall Details

Product Type
Drugs
Report Date
May 3, 2023
Initiation Date
March 16, 2023
Termination Date
N/A
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
a) 198 bottles; b) 22 bottles

Product Description

Glimepiride Tablets, USP 4mg, packaged in a) 30-count bottles (NDC 51655-120-52), and b) 90-count bottles (NDC 51655-120-26), Rx Only, Repackaged By: Northwind Pharmaceuticals, Indianapolis, IN 46203.

Reason for Recall

CGMP Deviations

Distribution Pattern

Nationwide with the United States

Code Information

a) Lot #: F105692201, Exp. Date 09/30/2024; F105692203, Exp. Date 02/28/2025 b) Lot #: F105692202, Exp. Date 02/28/2025