NDC 61699-0047

Solu-Medrol 125 mg per 1 mL injection, powder, for solution

On the label: US MedSource, LLC. It's repackaged: US MedSource, LLC rebottles it from Pharmacia & Upjohn Company LLC's NDC 0009-0047.

United States: 1

Where the pills inside were 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

Repackaging site

Product details

Generic drug
Methylprednisolone: every company that makes it
Form
injection, powder, for solution
Strength
125 mg per 1 mL
Approval
NDA NDA011856
On the market since
Jul 18, 2014
Package NDCs
61699-0047-2
Official label
DailyMed (National Library of Medicine), updated Jul 18, 2014

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