FDA Drug recall D-0485-2016
Prednisone 20 mg, Tablet, 10-count bottle, Rx only, Mfg by: HIKMA Pharmaceuticals PO BOX 182400 Amman 11118 Jordan
- FDA Drug
- Class III
- terminated
- Published 2015-12-09
On 2015-12-09 the FDA classified a Class III recall of Prednisone 20 mg, Tablet, 10-count bottle, Rx only, Mfg by: HIKMA Pharmaceuticals PO BOX 182400 Amman 11118 Jordan by Northwind Pharmaceuticals, citing labeling: Not elsewhere classified. NDC number is incorrect on the container.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0485-2016 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2015-11-10 |
| Published | 2015-12-09 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Northwind Pharmaceuticals |
| Distribution | US |
Product
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
Labeling: Not elsewhere classified. NDC number is incorrect on the container.
Identifiers
| code_info | Lot # NW 46400021, Exp 03/2018 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.
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FDA Drug · Class II · 2023-05-03 · Northwind Pharmaceuticals
All Northwind Pharmaceuticals recalls
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0485-2016%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.