NDC 42708-045
PredniSONE 10 mg tablet
On the label: QPharma, Inc.. It's repackaged: QPharma, Inc. rebottles it from Hikma Pharmaceuticals USA Inc.'s NDC 0054-0017.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| West-Ward Columbus Inc. | Columbus, OH, United States | Makes it | No problems foundApr 30, 2026 · 27 inspections |
Repackaging site
- Northwind Health Company, LLC, Indianapolis, IN, United States · repackages it
Recalls
- Oct 3, 2016 · Class II · West-Ward Pharmaceutical
Failed Tablet/Capsule Specifications: Discovery of an underweight tablet.
Lots: Lot # 660621A, Exp 01/31/18 - Jun 14, 2013 · Class III · Boehringer Ingelheim Roxane Inc
Labeling: Missing Label; missing label on blister card
Lots: The affected product consists of lot #261739A, expiration date OCT 2014.
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Prednisone: every company that makes it
- Form
- tablet, oral
- Strength
- 10 mg
- Approval
- ANDA ANDA084122
- On the market since
- Feb 13, 2003
- Package NDCs
42708-045-21- Official label
- DailyMed (National Library of Medicine), updated Dec 5, 2025
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