Approvals/TGA/SOLU-MEDROL methylprednisolone 500mg (as sodium succinate) powder for injection vial

Approved

STANDARD

SOLU-MEDROL methylprednisolone 500mg (as sodium succinate) powder for injection vial

Pfizer Australia Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: 2c8e056ded75e300
Product Name: SOLU-MEDROL methylprednisolone 500mg (as sodium succinate) powder for injection vial
Artg Id: 50691
Artg Name: SOLU-MEDROL methylprednisolone 500mg (as sodium succinate) powder for injection vial
Sponsor: Pfizer Australia Pty Ltd
Company Detail Path: /organization/pfizer-australia-pty-ltd
Artg Date: 1994-11-22
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE
Consumer Medicine Info: https://medical-cdn.nocode.com/drug_tga/c67ad6a433eba8cf52f0944a9b62240d.pdf
Product Information: https://medical-cdn.nocode.com/drug_tga/2b57451d28ea03ce1ca5c7f513d331fa.pdf

Approved

Agency

TGA

Country

🇦🇺

Approval Date

May 31, 2025

Approval ID

2c8e056ded75e300

Type

Standard