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TGA
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GEMCITABINE GxP gemcitabine (as hydrochloride) 200 mg powder for injection vial
Approved
STANDARD
GEMCITABINE GxP gemcitabine (as hydrochloride) 200 mg powder for injection vial
MedTAS Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
May 30, 2025
Approval ID
cd3580b56b328800
Company
MedTAS Pty Ltd
Type
Standard
Approval Details
Approval Id
cd3580b56b328800
Product Name
GEMCITABINE GxP gemcitabine (as hydrochloride) 200 mg powder for injection vial
Artg Id
207996
Artg Name
GEMCITABINE GxP gemcitabine (as hydrochloride) 200 mg powder for injection vial
Sponsor
MedTAS Pty Ltd
Company Detail Path
/organization/medtas-pty-ltd
Artg Date
2015-03-03
Registration Type
Medicine
Therapeutic Good Type
Medicine
Licence Status
A
Licence Category
RE
Active Ingredients
Approved
Quick Info
Agency
TGA
Country
🇦🇺
Approval Date
May 30, 2025
Approval ID
cd3580b56b328800
Type
Standard
Back to TGA Approvals
GEMCITABINE GxP gemcitabine (as hydrochloride) 200 mg powder for injection vial - TGA Drug Approval Details
