NDC 76420-413
prednisone 20 mg tablet
On the label: Asclemed USA, Inc.. It's repackaged: Asclemed USA, Inc. rebottles it from Strides Pharma Science Limited's NDC 64380-785.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Strides Pharma Science Limited | Bengaluru, India | Makes it, tests it and packages it | Problems found, fixed voluntarilyMay 20, 2026 · 11 inspections |
Repackaging site
- Asclemed USA Inc. dba Enovachem, Torrance, CA, United States · repackages it and relabels it
Recalls
- Jul 19, 2022 · Class II · Strides Pharma Inc.
Presence of foreign tablet: 2.5 mg tablet in a 20 mg bottle of Prednisone Tablets
Lots: Lot #: 7248988B, Exp 9/2023
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 ANDA208412
- On the market since
- Sep 1, 2021
- Package NDCs
76420-413-0076420-413-0176420-413-0576420-413-1076420-413-1876420-413-2076420-413-2176420-413-3076420-413-5076420-413-6076420-413-90- Official label
- DailyMed (National Library of Medicine), updated Mar 3, 2026
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