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ATROVENT NASAL ipratropium bromide monohydrate 22 microgram/actuation spray solution - TGA Drug Approval Details
Approvals
/
TGA
/
ATROVENT NASAL ipratropium bromide monohydrate 22 microgram/actuation spray solution
Approved
STANDARD
ATROVENT NASAL ipratropium bromide monohydrate 22 microgram/actuation spray solution
Sanofi-Aventis Healthcare Pty Ltd T/A Sanofi Consumer Healthcare
🇦🇺 Therapeutic Goods Administration
Approval Date
May 31, 2025
Approval ID
cbe50040324ff8ad
Company
Sanofi-Aventis Healthcare Pty Ltd T/A Sanofi Consumer Healthcare
Type
Standard
Approval Details
Approval Id
cbe50040324ff8ad
Product Name
ATROVENT NASAL ipratropium bromide monohydrate 22 microgram/actuation spray solution
Artg Id
53362
Artg Name
ATROVENT NASAL ipratropium bromide monohydrate 22 microgram/actuation spray solution
Sponsor
Sanofi-Aventis Healthcare Pty Ltd T/A Sanofi Consumer Healthcare
Company Detail Path
/organization/sanofi-aventis-healthcare-pty-ltd
Artg Date
1995-08-30
Registration Type
Medicine
Therapeutic Good Type
Medicine
Licence Status
A
Licence Category
RE
Consumer Medicine Info
https://medical-cdn.nocode.com/drug_tga/fb37d2a90b5d905d014f0f75d24a77eb.pdf
Active Ingredients
Approved
Quick Info
Agency
TGA
Country
🇦🇺
Approval Date
May 31, 2025
Approval ID
cbe50040324ff8ad
Type
Standard
Back to TGA Approvals