Prednisone 20 mg, Tablet, 10-count bottle, Rx only, Mfg by: HIKMA Pharmaceuticals PO BOX 182400 A...

FDA Recall #D-0485-2016 — Class III — November 10, 2015

Recall #D-0485-2016 Date: November 10, 2015 Classification: Class III Status: Terminated

Product Description

Prednisone 20 mg, Tablet, 10-count bottle, Rx only, Mfg by: HIKMA Pharmaceuticals PO BOX 182400 Amman 11118 Jordan. Dist By: West-Ward Pharmaceuticals Corp., Eatentown, NJ 07724 USA, Repackaged By: Northwind Pharmaceuticals, Indianapolis, IN 46256. NDC 51655-320-53

Reason for Recall

Labeling: Not elsewhere classified. NDC number is incorrect on the container.

Recalling Firm

Northwind Pharmaceuticals LLC — Indianapolis, IN

Classification

Class III — Not likely to cause adverse health consequences.

Product Type

Drugs

Product Quantity

40 Bottles

Distribution

Nationwide

Code Information

Lot # NW 46400021, Exp 03/2018

Status

Terminated

Voluntary / Mandated

Voluntary: Firm initiated