PlainRecalls
FDA Drug Low Class III Terminated

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

Reported: December 9, 2015 Initiated: November 10, 2015 #D-0485-2016

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.

Details

Units Affected
40 Bottles
Distribution
Nationwide
Location
Indianapolis, IN

Frequently Asked Questions

What product was recalled?
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. Recalled by Northwind Pharmaceuticals LLC. Units affected: 40 Bottles.
Why was this product recalled?
Labeling: Not elsewhere classified. NDC number is incorrect on the container.
Which agency issued this recall?
This recall was issued by the FDA Drug on December 9, 2015. Severity: Low. Recall number: D-0485-2016.