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VUMERITY diroximel fumarate 231 mg enteric capsules bottle - TGA Drug Approval Details
Approvals
/
TGA
/
VUMERITY diroximel fumarate 231 mg enteric capsules bottle
Approved
STANDARD
VUMERITY diroximel fumarate 231 mg enteric capsules bottle
Biogen Australia Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
May 30, 2025
Approval ID
d3a52991dfddd952
Company
Biogen Australia Pty Ltd
Type
Standard
Approval Details
Approval Id
d3a52991dfddd952
Product Name
VUMERITY diroximel fumarate 231 mg enteric capsules bottle
Artg Id
354530
Artg Name
VUMERITY diroximel fumarate 231 mg enteric capsules bottle
Sponsor
Biogen Australia Pty Ltd
Company Detail Path
/organization/biogen-australia-pty-ltd
Artg Date
2022-03-21
Registration Type
Medicine
Therapeutic Good Type
Medicine
Licence Status
A
Licence Category
RE
Consumer Medicine Info
https://medical-cdn.nocode.com/drug_tga/88b1a4876839a160cd429c28d2cbdd98.pdf
Product Information
https://medical-cdn.nocode.com/drug_tga/857da8f1bdce25127c850a79bee1be30.pdf
Active Ingredients
Approved
Quick Info
Agency
TGA
Country
🇦🇺
Approval Date
May 30, 2025
Approval ID
d3a52991dfddd952
Type
Standard
Back to TGA Approvals