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BUDAMAX AQUEOUS NASAL SPRAY budesonide 32 microgram/actuation spray bottle - TGA Drug Approval Details
Approvals
/
TGA
/
BUDAMAX AQUEOUS NASAL SPRAY budesonide 32 microgram/actuation spray bottle
Approved
STANDARD
BUDAMAX AQUEOUS NASAL SPRAY budesonide 32 microgram/actuation spray bottle
Johnson & Johnson Pacific Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
May 30, 2025
Approval ID
dbb00b8e6b2556df
Company
Johnson & Johnson Pacific Pty Ltd
Type
Standard
Approval Details
Approval Id
dbb00b8e6b2556df
Product Name
BUDAMAX AQUEOUS NASAL SPRAY budesonide 32 microgram/actuation spray bottle
Artg Id
75657
Artg Name
BUDAMAX AQUEOUS NASAL SPRAY budesonide 32 microgram/actuation spray bottle
Sponsor
Johnson & Johnson Pacific Pty Ltd
Company Detail Path
/organization/johnson-and-johnson-pacific-pty-ltd
Artg Date
2000-08-24
Registration Type
Medicine
Therapeutic Good Type
Medicine
Licence Status
A
Licence Category
RE
Consumer Medicine Info
https://medical-cdn.nocode.com/drug_tga/134b40d214d06dde96159480a7d1a725.pdf
Active Ingredients
Approved
Quick Info
Agency
TGA
Country
🇦🇺
Approval Date
May 30, 2025
Approval ID
dbb00b8e6b2556df
Type
Standard
Back to TGA Approvals