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Last Updated: December 18, 2025

Details for New Drug Application (NDA): 011856


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NDA 011856 describes SOLU-MEDROL, which is a drug marketed by Pharmacia And Upjohn and is included in one NDA. It is available from nine suppliers. Additional details are available on the SOLU-MEDROL profile page.

The generic ingredient in SOLU-MEDROL is methylprednisolone sodium succinate. There are forty drug master file entries for this compound. Sixteen suppliers are listed for this compound. Additional details are available on the methylprednisolone sodium succinate profile page.
Summary for 011856
Tradename:SOLU-MEDROL
Applicant:Pharmacia And Upjohn
Ingredient:methylprednisolone sodium succinate
Patents:0
Pharmacology for NDA: 011856
Mechanism of ActionCorticosteroid Hormone Receptor Agonists
Suppliers and Packaging for NDA: 011856
Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
SOLU-MEDROL methylprednisolone sodium succinate INJECTABLE;INJECTION 011856 NDA Pharmacia & Upjohn Company LLC 0009-0003 0009-0003-02 1 VIAL in 1 CARTON (0009-0003-02) / 4 mL in 1 VIAL
SOLU-MEDROL methylprednisolone sodium succinate INJECTABLE;INJECTION 011856 NDA Pharmacia & Upjohn Company LLC 0009-0018 0009-0018-20 1 VIAL in 1 CARTON (0009-0018-20) / 8 mL in 1 VIAL

Profile for product number 003

Active Rx/OTC/Discontinued:RXDosage:INJECTABLE;INJECTIONStrengthEQ 40MG BASE/VIAL
Approval Date:Approved Prior to Jan 1, 1982TE:APRLD:Yes

Profile for product number 004

Active Rx/OTC/Discontinued:RXDosage:INJECTABLE;INJECTIONStrengthEQ 125MG BASE/VIAL
Approval Date:Approved Prior to Jan 1, 1982TE:APRLD:Yes

Profile for product number 005

Active Rx/OTC/Discontinued:RXDosage:INJECTABLE;INJECTIONStrengthEQ 500MG BASE/VIAL
Approval Date:Approved Prior to Jan 1, 1982TE:APRLD:Yes

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Preferred Citation:

Friedman, Yali. "DrugPatentWatch" DrugPatentWatch, thinkBiotech, 2025, www.DrugPatentWatch.com.
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