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SANDOZ FESOTERODINE FUMARATE - Health Canada Drug Approval Details
Approvals
/
Health Canada
/
SANDOZ FESOTERODINE FUMARATE
Authorized
STANDARD
SANDOZ FESOTERODINE FUMARATE
Sandoz Canada, Inc.
🇨🇦 Health Canada
Approval Date
Jul 4, 2025
Approval ID
71049669bda7d763
Company
Sandoz Canada, Inc.
Type
Standard
Approval Details
Approval Id
71049669bda7d763
Drug Approval Canada Name
SANDOZ FESOTERODINE FUMARATE
Product Name
SANDOZ FESOTERODINE FUMARATE
Status
Marketed
Status Date
2022-05-02
Original Market Date
2022-05-02
Din
02521768
Drug Class
Human
Dosage Form
Tablet (Extended-Release)
Route Of Administration
Oral
Schedule
Prescription
Ahfs
86:12.04
Atc Original
G04BD11 FESOTERODINE
Atc Name
g 04 bd 11
Aig Number
0153091001
Company Name
Sandoz Canada, Inc.
Company Address
4600 Rue Armand-Frappier, Saint-Hubert, Quebec, Canada, J3Z 1G5
Company Detail Path
/organization/sandoz-canada-inc
Company Information
Pharmaceutical Company Name
Sandoz Canada, Inc.
Country Name
Canada
Website
http://www.sandoz.ca
Active Ingredients
FESOTERODINE FUMARATE
4 MG
Authorized
Quick Info
Agency
Health Canada
Country
🇨🇦
Approval Date
Jul 4, 2025
Approval ID
71049669bda7d763
Type
Standard
Back to Health Canada Approvals