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ALENDRO ONCE-WEEKLY alendronic acid 70 mg (as sodium alendronate monohydrate) tablet blister pack - TGA Drug Approval Details
Approvals
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TGA
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ALENDRO ONCE-WEEKLY alendronic acid 70 mg (as sodium alendronate monohydrate) tablet blister pack
Approved
STANDARD
ALENDRO ONCE-WEEKLY alendronic acid 70 mg (as sodium alendronate monohydrate) tablet blister pack
Arrotex Pharmaceuticals Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
Dec 9, 2025
Approval ID
d7a7c3af2a9a8268
Company
Arrotex Pharmaceuticals Pty Ltd
Type
Standard
Approval Details
Approval Id
d7a7c3af2a9a8268
Product Name
ALENDRO ONCE-WEEKLY alendronic acid 70 mg (as sodium alendronate monohydrate) tablet blister pack
Artg Id
100691
Artg Name
ALENDRO ONCE-WEEKLY alendronic acid 70 mg (as sodium alendronate monohydrate) tablet blister pack
Sponsor
Arrotex Pharmaceuticals Pty Ltd
Company Detail Path
/organization/arrotex-pharmaceuticals-pty-ltd
Artg Date
2005-05-27
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
d7a7c3af2a9a8268
Type
Standard
Back to TGA Approvals