SOLU-MEDROL (METHYLPREDNISOLONE SODIUM SUCCINATE)
Summary
FDA approved SOLU-MEDROL (METHYLPREDNISOLONE SODIUM SUCCINATE) by PHARMACIA AND UPJOHN. NDA (New Drug) approval (Labeling) on 2025-11-04. INJECTABLE, INJECTION.
Details
Source
Drug Approval
External ID
NDA011856-143
Action Date
2025-11-04
Status
Approved
Category
drug
Product Code
NDA (New Drug)
Product Description
SOLU-MEDROL (generic: METHYLPREDNISOLONE SODIUM SUCCINATE), INJECTABLE, INJECTION. Application: NDA011856
Company
Context & Analysis
Frequently Asked Questions
How often does PHARMACIA AND UPJOHN have FDA actions?
This is the only FDA action we have on record for PHARMACIA AND UPJOHN in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "NDA011856-143" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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