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HEIDI-35 ED tablet blister pack - TGA Drug Approval Details
Approvals
/
TGA
/
HEIDI-35 ED tablet blister pack
Approved
STANDARD
HEIDI-35 ED tablet blister pack
GM Pharma International Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
May 30, 2025
Approval ID
f7ce8c5eeda96640
Company
GM Pharma International Pty Ltd
Type
Standard
Approval Details
Approval Id
f7ce8c5eeda96640
Product Name
HEIDI-35 ED tablet blister pack
Artg Id
422046
Artg Name
HEIDI-35 ED tablet blister pack
Sponsor
GM Pharma International Pty Ltd
Company Detail Path
/organization/gm-pharma-international-pty-ltd
Artg Date
2024-01-03
Registration Type
Medicine
Therapeutic Good Type
Medicine
Licence Status
A
Licence Category
RE
Consumer Medicine Info
https://medical-cdn.nocode.com/drug_tga/067a7a7dfcc40fc39d04d95601be3c77.pdf
Product Information
https://medical-cdn.nocode.com/drug_tga/77be25a15eb1d29a87918b69a9d329e6.pdf
Active Ingredients
Approved
Quick Info
Agency
TGA
Country
🇦🇺
Approval Date
May 30, 2025
Approval ID
f7ce8c5eeda96640
Type
Standard
Back to TGA Approvals