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APO-ZIPRASIDONE ziprasidone (as hydrochloride) 40 mg capsule bottle - TGA Drug Approval Details
Approvals
/
TGA
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APO-ZIPRASIDONE ziprasidone (as hydrochloride) 40 mg capsule bottle
Approved
STANDARD
APO-ZIPRASIDONE ziprasidone (as hydrochloride) 40 mg capsule bottle
Arrotex Pharmaceuticals Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
May 29, 2025
Approval ID
08660e6689c13b26
Company
Arrotex Pharmaceuticals Pty Ltd
Type
Standard
Approval Details
Approval Id
08660e6689c13b26
Product Name
APO-ZIPRASIDONE ziprasidone (as hydrochloride) 40 mg capsule bottle
Artg Id
201053
Artg Name
APO-ZIPRASIDONE ziprasidone (as hydrochloride) 40 mg capsule bottle
Sponsor
Arrotex Pharmaceuticals Pty Ltd
Company Detail Path
/organization/arrotex-pharmaceuticals-pty-ltd
Artg Date
2013-08-13
Registration Type
Medicine
Therapeutic Good Type
Medicine
Licence Status
A
Licence Category
RE
Active Ingredients
Approved
Quick Info
Agency
TGA
Country
🇦🇺
Approval Date
May 29, 2025
Approval ID
08660e6689c13b26
Type
Standard
Back to TGA Approvals
