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GEMCITABINE SANDOZ gemcitabine (as hydrochloride) 500 mg/50 mL concentrated solution for infusion vial - TGA Drug Approval Details
Approvals
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TGA
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GEMCITABINE SANDOZ gemcitabine (as hydrochloride) 500 mg/50 mL concentrated solution for infusion vial
Approved
STANDARD
GEMCITABINE SANDOZ gemcitabine (as hydrochloride) 500 mg/50 mL concentrated solution for infusion vial
Sandoz Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
Dec 9, 2025
Approval ID
fd17f6fa688338ca
Company
Sandoz Pty Ltd
Type
Standard
Approval Details
Approval Id
fd17f6fa688338ca
Product Name
GEMCITABINE SANDOZ gemcitabine (as hydrochloride) 500 mg/50 mL concentrated solution for infusion vial
Artg Id
146762
Artg Name
GEMCITABINE SANDOZ gemcitabine (as hydrochloride) 500 mg/50 mL concentrated solution for infusion vial
Sponsor
Sandoz Pty Ltd
Company Detail Path
/organization/sandoz-pty-ltd
Artg Date
2008-12-02
Registration Type
Medicine
Therapeutic Good Type
Medicine
Licence Status
A
Licence Category
RE
Approved
Quick Info
Agency
TGA
Country
🇦🇺
Approval Date
Dec 9, 2025
Approval ID
fd17f6fa688338ca
Type
Standard
Back to TGA Approvals