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AMLODIPINE/VALSARTAN/HCT NOVARTIS 10/320/25 amlodipine/valsartan/hydrochlorothiazide tablet blister pack - TGA Drug Approval Details
Approvals
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TGA
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AMLODIPINE/VALSARTAN/HCT NOVARTIS 10/320/25 amlodipine/valsartan/hydrochlorothiazide tablet blister pack
Approved
STANDARD
AMLODIPINE/VALSARTAN/HCT NOVARTIS 10/320/25 amlodipine/valsartan/hydrochlorothiazide tablet blister pack
Novartis Pharmaceuticals Australia Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
May 30, 2025
Approval ID
46f27af77e200d7b
Company
Novartis Pharmaceuticals Australia Pty Ltd
Type
Standard
Approval Details
Approval Id
46f27af77e200d7b
Product Name
AMLODIPINE/VALSARTAN/HCT NOVARTIS 10/320/25 amlodipine/valsartan/hydrochlorothiazide tablet blister pack
Artg Id
158169
Artg Name
AMLODIPINE/VALSARTAN/HCT NOVARTIS 10/320/25 amlodipine/valsartan/hydrochlorothiazide tablet blister pack
Sponsor
Novartis Pharmaceuticals Australia Pty Ltd
Company Detail Path
/organization/novartis-pharmaceuticals-australia-pty-ltd
Artg Date
2010-04-09
Registration Type
Medicine
Therapeutic Good Type
Medicine
Licence Status
A
Licence Category
RE
Consumer Medicine Info
https://medical-cdn.nocode.com/drug_tga/b7cb53896118368fe63dec5fe9c85df6.pdf
Product Information
https://medical-cdn.nocode.com/drug_tga/2b9bb60388a249727ec90744fbb5743f.pdf
Active Ingredients
Approved
Quick Info
Agency
TGA
Country
🇦🇺
Approval Date
May 30, 2025
Approval ID
46f27af77e200d7b
Type
Standard
Back to TGA Approvals