NDC 68071-2370
Methylprednisolone 4 mg tablet
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Mylan Pharmaceuticals Inc.'s NDC 59762-4440.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Pfizer Italia S.r.l. | Ascoli Piceno, Italy | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyMar 14, 2025 · 5 inspections |
| Pharmacia & Upjohn Company LLC | Kalamazoo, MI, United States | Makes it, makes the active ingredient and tests it | Problems found, fixed voluntarilyJun 16, 2023 · 9 inspections |
Repackaging site
- NuCare Pharmaceuticals,Inc., Orange, CA, United States · relabels it
Recalls
- Jan 15, 2026 · Class II · Greenstone Llc
Labeling: Not Elsewhere Classified. Incorrect orientation of the blister foil applied to the blister cavities, which results in incorrect dosing information when following the directions on the foil.
Lots: Lot # LG7675, Exp. Date Nov 2026
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Methylprednisolone: every company that makes it
- Form
- tablet, oral
- Strength
- 4 mg
- Approval
- NDA authorized generic NDA011153
- On the market since
- Oct 11, 2011
- Package NDCs
68071-2370-1- Official label
- DailyMed (National Library of Medicine), updated Feb 20, 2026
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