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RHINOCORT HAYFEVER & ALLERGY ORIGINAL budesonide 32ug actuation nasal spray - TGA Drug Approval Details
Approvals
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TGA
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RHINOCORT HAYFEVER & ALLERGY ORIGINAL budesonide 32ug actuation nasal spray
Approved
STANDARD
RHINOCORT HAYFEVER & ALLERGY ORIGINAL budesonide 32ug actuation nasal spray
Johnson & Johnson Pacific Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
May 30, 2025
Approval ID
185fd588d43c5a62
Company
Johnson & Johnson Pacific Pty Ltd
Type
Standard
Approval Details
Approval Id
185fd588d43c5a62
Product Name
RHINOCORT HAYFEVER & ALLERGY ORIGINAL budesonide 32ug actuation nasal spray
Artg Id
77885
Artg Name
RHINOCORT HAYFEVER & ALLERGY ORIGINAL budesonide 32ug actuation nasal spray
Sponsor
Johnson & Johnson Pacific Pty Ltd
Company Detail Path
/organization/johnson-and-johnson-pacific-pty-ltd
Artg Date
2001-05-03
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
185fd588d43c5a62
Type
Standard
Back to TGA Approvals
