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PRICELINE IBUPROFEN LIQUID CAPSULES 200 mg soft gelatin capsule blister pack
Approved
STANDARD
PRICELINE IBUPROFEN LIQUID CAPSULES 200 mg soft gelatin capsule blister pack
Nova Pharmaceuticals Australasia Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
May 30, 2025
Approval ID
e77c8722c7339599
Company
Nova Pharmaceuticals Australasia Pty Ltd
Type
Standard
Approval Details
Approval Id
e77c8722c7339599
Product Name
PRICELINE IBUPROFEN LIQUID CAPSULES 200 mg soft gelatin capsule blister pack
Artg Id
307059
Artg Name
PRICELINE IBUPROFEN LIQUID CAPSULES 200 mg soft gelatin capsule blister pack
Sponsor
Nova Pharmaceuticals Australasia Pty Ltd
Company Detail Path
/organization/nova-pharmaceuticals-australasia-pty-ltd
Artg Date
2018-07-16
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
e77c8722c7339599
Type
Standard
Back to TGA Approvals
PRICELINE IBUPROFEN LIQUID CAPSULES 200 mg soft gelatin capsule blister pack - TGA Drug Approval Details
