NDC 52959-126
Prednisone 10 mg tablet
On the label: H.J. Harkins Co., Inc.. It's repackaged: H.J. Harkins Co., Inc. rebottles it from Par Health USA, LLC's NDC 0603-5338.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Generics Bidco II LLC d/b/a Prinston Laboratories | Charlotte, NC, United States | Makes it, packages it and labels it | Problems found, fixed voluntarilySep 19, 2025 · 10 inspections, 1 with FDA action |
| Generics Bidco II LLC d/b/a Prinston Laboratories | Charlotte, NC, United States | Makes it and tests it | Problems found, fixed voluntarilySep 19, 2025 · 10 inspections, 1 with FDA action |
| Par Formulations Private Limited | Chennai, India | Makes it, tests it and packages it | Problems found, fixed voluntarilyJun 10, 2026 · 7 inspections |
Recalls
- Mar 4, 2020 · Class III · Par Pharmaceutical Inc.
Labeling: Incorrect or Missing Exp Date - An incorrect expiration date has been identified on Prednisone Tablets USP 5 mg
Lots: Lot #: 8672518, Exp 12/21
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
- Strength
- 10 mg
- Approval
- ANDA ANDA040256
- On the market since
- Jul 12, 2002
- Package NDCs
52959-126-0052959-126-0552959-126-0752959-126-1052959-126-1252959-126-1452959-126-1552959-126-1852959-126-2052959-126-2152959-126-2552959-126-30- Official label
- DailyMed (National Library of Medicine), updated Nov 4, 2011
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