# FDA recall D-0485-2016

> **Northwind Pharmaceuticals LLC** · Class III · drug recall initiated 2015-11-10.

## 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.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-0485-2016
- **Recalling firm:** Northwind Pharmaceuticals LLC
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2015-11-10
- **Report date:** 2015-12-09
- **Termination date:** 2017-03-29

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Indianapolis, IN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0485-2016

## Citation

> AI Analytics. FDA recall D-0485-2016. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/D-0485-2016. Source: US FDA. Licensed CC0.

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