NDC 68788-4182
PredniSONE 20 mg tablet
On the label: Preferred Pharmaceuticals, Inc... It's repackaged: Preferred Pharmaceuticals, Inc.. rebottles it from Hikma Pharmaceuticals USA Inc.'s NDC 0054-0018.
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
- Preferred Pharmaceuticals Inc., Anaheim, CA, 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
- 20 mg
- Approval
- ANDA ANDA080352
- On the market since
- Aug 20, 2026
- Package NDCs
68788-4182-168788-4182-268788-4182-368788-4182-468788-4182-568788-4182-8- Official label
- DailyMed (National Library of Medicine), updated Aug 20, 2026
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