NDC 42708-195
Prednisone 20 mg tablet
On the label: QPharma, Inc.. It's repackaged: QPharma, Inc. rebottles it from Aurobindo Pharma Limited's NDC 59651-488.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Apl Healthcare Limited | Tirupati, India | Makes it and tests it | Problems found, fixed voluntarilyDec 17, 2025 · 5 inspections |
Repackaging site
- Northwind Health Company, LLC, Indianapolis, IN, United States · repackages it
Product details
- Generic drug
- Prednisone: every company that makes it
- Form
- tablet, oral
- Strength
- 20 mg
- Approval
- ANDA ANDA215672
- On the market since
- Mar 28, 2022
- Package NDCs
42708-195-10- Official label
- DailyMed (National Library of Medicine), updated Feb 13, 2026
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