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VELETRI epoprostenol (as sodium) 1.5 mg powder for injection vial - TGA Drug Approval Details
Approvals
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TGA
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VELETRI epoprostenol (as sodium) 1.5 mg powder for injection vial
Approved
STANDARD
VELETRI epoprostenol (as sodium) 1.5 mg powder for injection vial
Janssen-Cilag Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
Dec 9, 2025
Approval ID
b070f5942a5d477e
Company
Janssen-Cilag Pty Ltd
Type
Standard
Approval Details
Approval Id
b070f5942a5d477e
Product Name
VELETRI epoprostenol (as sodium) 1.5 mg powder for injection vial
Artg Id
207547
Artg Name
VELETRI epoprostenol (as sodium) 1.5 mg powder for injection vial
Sponsor
Janssen-Cilag Pty Ltd
Company Detail Path
/organization/janssen-cilag-pty-ltd
Artg Date
2014-02-28
Registration Type
Medicine
Therapeutic Good Type
Medicine
Licence Status
A
Licence Category
RE
Consumer Medicine Info
https://medical-cdn.nocode.com/drug_tga/a79a4d8385693775e2097898ceb60885.pdf
Product Information
https://medical-cdn.nocode.com/drug_tga/118aab5fa0637e85ba6feef80a258ae9.pdf
Approved
Quick Info
Agency
TGA
Country
🇦🇺
Approval Date
Dec 9, 2025
Approval ID
b070f5942a5d477e
Type
Standard
Back to TGA Approvals