跳至主要内容
MedPath Trial Home
临床试验
产品
机构
资讯
AI 研究
价格
Search
EN
登录
我们重视您的隐私
我们使用 Cookie 分析网站流量并改善您的体验。请参阅我们的
隐私政策
。
拒绝
接受
Approvals
/
TGA
/
PEXOLE pramipexole dihydrochloride 0.125 mg tablets blister pack
Approved
STANDARD
PEXOLE pramipexole dihydrochloride 0.125 mg tablets blister pack
Arrotex Pharmaceuticals Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
May 28, 2025
Approval ID
43f58c0a0c77bb96
Company
Arrotex Pharmaceuticals Pty Ltd
Type
Standard
Approval Details
Approval Id
43f58c0a0c77bb96
Product Name
PEXOLE pramipexole dihydrochloride 0.125 mg tablets blister pack
Artg Id
214442
Artg Name
PEXOLE pramipexole dihydrochloride 0.125 mg tablets blister pack
Sponsor
Arrotex Pharmaceuticals Pty Ltd
Company Detail Path
/organization/arrotex-pharmaceuticals-pty-ltd
Artg Date
2014-09-23
Registration Type
Medicine
Therapeutic Good Type
Medicine
Licence Status
A
Licence Category
RE
Active Ingredients
Approved
Quick Info
Agency
TGA
Country
🇦🇺
Approval Date
May 28, 2025
Approval ID
43f58c0a0c77bb96
Type
Standard
Back to TGA Approvals
PEXOLE pramipexole dihydrochloride 0.125 mg tablets blister pack - TGA Drug Approval Details
