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SIMPONI golimumab (rmc) 50 mg/4 mL concentrate for solution for infusion vial - TGA Drug Approval Details
Approvals
/
TGA
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SIMPONI golimumab (rmc) 50 mg/4 mL concentrate for solution for infusion vial
Approved
STANDARD
SIMPONI golimumab (rmc) 50 mg/4 mL concentrate for solution for infusion vial
Janssen-Cilag Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
May 30, 2025
Approval ID
358831d09d2b51a0
Company
Janssen-Cilag Pty Ltd
Type
Standard
Approval Details
Approval Id
358831d09d2b51a0
Product Name
SIMPONI golimumab (rmc) 50 mg/4 mL concentrate for solution for infusion vial
Artg Id
311990
Artg Name
SIMPONI golimumab (rmc) 50 mg/4 mL concentrate for solution for infusion vial
Sponsor
Janssen-Cilag Pty Ltd
Company Detail Path
/organization/janssen-cilag-pty-ltd
Artg Date
2019-11-20
Registration Type
Medicine
Therapeutic Good Type
Medicine
Licence Status
A
Licence Category
RE
Consumer Medicine Info
https://medical-cdn.nocode.com/drug_tga/9c345edf04595b0b487c5b9191bdc7fd.pdf
Product Information
https://medical-cdn.nocode.com/drug_tga/1c19850e951d955961df68370dffc53a.pdf
Active Ingredients
Approved
Quick Info
Agency
TGA
Country
🇦🇺
Approval Date
May 30, 2025
Approval ID
358831d09d2b51a0
Type
Standard
Back to TGA Approvals