Prednisone 20 mg — Class III drug recall D-0485-2016
Terminated recall by Northwind Pharmaceuticals LLC, reported 2015-12-09, distributed nationwide. Labeling: Not elsewhere classified. NDC number is incorrect on the container.
| Recall number | D-0485-2016 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Northwind Pharmaceuticals LLC, Indianapolis, IN, United States |
| Recall initiated | 2015-11-10 |
| Classified | 2015-12-02 |
| Reported by FDA | 2015-12-09 |
| Terminated | 2017-03-29 |
| Distributed | Nationwide (US) |
| Quantity | 40 bottles |
| Reason classes | labeling |
| NDC | 51655-0320-53 |
| Lot numbers | 46400021 |
| Expiration dates | 2018-03 |
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 for recall
Labeling: Not elsewhere classified. NDC number is incorrect on the container.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0485-2016. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.