NDC 0009-0047

Solu-Medrol 125 mg per 2 mL injection, powder, for solution

On the label: Pharmacia & Upjohn Company LLC.

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Pharmacia & Upjohn Company LLCKalamazoo, MI, United StatesMakes it, makes the active ingredient, tests it, packages it and labels it Problems found, fixed voluntarilyJun 16, 2023 · 9 inspections

Product details

Generic drug
Methylprednisolone: every company that makes it
Form
injection, powder, for solution, intramuscular; intravenous
Strength
125 mg per 2 mL
Approval
NDA NDA011856
On the market since
Apr 2, 1959
Package NDCs
0009-0047-03 0009-0047-04
Official label
DailyMed (National Library of Medicine), updated Jun 25, 2026

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