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NEUPRO rotigotine 3 mg/24 hr transdermal patch sachet - TGA Drug Approval Details
Approvals
/
TGA
/
NEUPRO rotigotine 3 mg/24 hr transdermal patch sachet
Approved
STANDARD
NEUPRO rotigotine 3 mg/24 hr transdermal patch sachet
UCB Australia Pty Ltd T/A UCB Pharma Division of UCB Australia
🇦🇺 Therapeutic Goods Administration
Approval Date
Dec 9, 2025
Approval ID
46036d48a40d69d6
Company
UCB Australia Pty Ltd T/A UCB Pharma Division of UCB Australia
Type
Standard
Approval Details
Approval Id
46036d48a40d69d6
Product Name
NEUPRO rotigotine 3 mg/24 hr transdermal patch sachet
Artg Id
163988
Artg Name
NEUPRO rotigotine 3 mg/24 hr transdermal patch sachet
Sponsor
UCB Australia Pty Ltd T/A UCB Pharma Division of UCB Australia
Company Detail Path
/organization/ucb-australia-pty-ltd
Artg Date
2010-10-19
Registration Type
Medicine
Therapeutic Good Type
Medicine
Licence Status
A
Licence Category
RE
Product Information
https://medical-cdn.nocode.com/drug_tga/b7ce8172046353f81632db7455a100a0.pdf
Approved
Quick Info
Agency
TGA
Country
🇦🇺
Approval Date
Dec 9, 2025
Approval ID
46036d48a40d69d6
Type
Standard
Back to TGA Approvals