NDC 17856-3722
PredniSONE 5 mg per 5 mL solution
On the label: Atlantic Biologicals Corps.. It's repackaged: Atlantic Biologicals Corps. rebottles it from Hikma Pharmaceuticals USA Inc.'s NDC 0054-3722.
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
- Unit Dose Solutions, Inc., Raleigh, NC, 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
- solution, oral
- Strength
- 5 mg per 5 mL
- Approval
- ANDA ANDA088703
- On the market since
- Dec 13, 1986
- Package NDCs
17856-3722-117856-3722-217856-3722-3- Official label
- DailyMed (National Library of Medicine), updated Sep 29, 2026
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