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CITALOPRAM-ARX citalopram 20 mg (as hydrobromide) tablet bottle - TGA Drug Approval Details
Approvals
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TGA
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CITALOPRAM-ARX citalopram 20 mg (as hydrobromide) tablet bottle
Approved
STANDARD
CITALOPRAM-ARX citalopram 20 mg (as hydrobromide) tablet bottle
Arrotex Pharmaceuticals Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
May 30, 2025
Approval ID
a0de72a2107fdca9
Company
Arrotex Pharmaceuticals Pty Ltd
Type
Standard
Approval Details
Approval Id
a0de72a2107fdca9
Product Name
CITALOPRAM-ARX citalopram 20 mg (as hydrobromide) tablet bottle
Artg Id
337475
Artg Name
CITALOPRAM-ARX citalopram 20 mg (as hydrobromide) tablet bottle
Sponsor
Arrotex Pharmaceuticals Pty Ltd
Company Detail Path
/organization/arrotex-pharmaceuticals-pty-ltd
Artg Date
2020-06-23
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
a0de72a2107fdca9
Type
Standard
Back to TGA Approvals
