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LUROBI lurasidone hydrochloride 20 mg film-coated tablet blister pack - TGA Drug Approval Details
Approvals
/
TGA
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LUROBI lurasidone hydrochloride 20 mg film-coated tablet blister pack
Approved
STANDARD
LUROBI lurasidone hydrochloride 20 mg film-coated tablet blister pack
Alembic Pharmaceuticals Australia Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
May 29, 2025
Approval ID
0edab4755c4d86cf
Company
Alembic Pharmaceuticals Australia Pty Ltd
Type
Standard
Approval Details
Approval Id
0edab4755c4d86cf
Product Name
LUROBI lurasidone hydrochloride 20 mg film-coated tablet blister pack
Artg Id
436650
Artg Name
LUROBI lurasidone hydrochloride 20 mg film-coated tablet blister pack
Sponsor
Alembic Pharmaceuticals Australia Pty Ltd
Company Detail Path
/organization/alembic-pharmaceuticals-australia-pty-ltd
Artg Date
2024-04-17
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
0edab4755c4d86cf
Type
Standard
Back to TGA Approvals
