NDC 68071-2661
Prednisone 10 mg tablet
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Strides Pharma Science Limited's NDC 64380-784.
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
- NuCare Pharmaceuticals,Inc., Orange, CA, United States · repackages 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
- 10 mg
- Approval
- ANDA ANDA208412
- On the market since
- Sep 1, 2021
- Package NDCs
68071-2661-068071-2661-168071-2661-268071-2661-368071-2661-568071-2661-6- Official label
- DailyMed (National Library of Medicine), updated Apr 23, 2024
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?