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PANTOPRAZOLE-AFT pantoprazole (as sodium sesquihydrate) 40 mg powder for injection vial - TGA Drug Approval Details
Approvals
/
TGA
/
PANTOPRAZOLE-AFT pantoprazole (as sodium sesquihydrate) 40 mg powder for injection vial
Approved
STANDARD
PANTOPRAZOLE-AFT pantoprazole (as sodium sesquihydrate) 40 mg powder for injection vial
AFT Pharmaceuticals Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
May 30, 2025
Approval ID
ef6b8ce9ffd8d962
Company
AFT Pharmaceuticals Pty Ltd
Type
Standard
Approval Details
Approval Id
ef6b8ce9ffd8d962
Product Name
PANTOPRAZOLE-AFT pantoprazole (as sodium sesquihydrate) 40 mg powder for injection vial
Artg Id
288085
Artg Name
PANTOPRAZOLE-AFT pantoprazole (as sodium sesquihydrate) 40 mg powder for injection vial
Sponsor
AFT Pharmaceuticals Pty Ltd
Company Detail Path
/organization/aft-pharmaceuticals-au-pty-ltd
Artg Date
2018-08-02
Registration Type
Medicine
Therapeutic Good Type
Medicine
Licence Status
A
Licence Category
RE
Consumer Medicine Info
https://medical-cdn.nocode.com/drug_tga/911e265f68382f651b253af4e118d6bc.pdf
Product Information
https://medical-cdn.nocode.com/drug_tga/5ae0c62f21ef22c2959da523a2134fe3.pdf
Active Ingredients
Approved
Quick Info
Agency
TGA
Country
🇦🇺
Approval Date
May 30, 2025
Approval ID
ef6b8ce9ffd8d962
Type
Standard
Back to TGA Approvals