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SANDOZ FLUOXETINE - Health Canada Drug Approval Details
Approvals
/
Health Canada
/
SANDOZ FLUOXETINE
Authorized
STANDARD
SANDOZ FLUOXETINE
Sandoz Canada, Inc.
🇨🇦 Health Canada
Approval Date
Jul 4, 2025
Approval ID
ad613651e3224133
Company
Sandoz Canada, Inc.
Type
Standard
Approval Details
Approval Id
ad613651e3224133
Drug Approval Canada Name
SANDOZ FLUOXETINE
Product Name
SANDOZ FLUOXETINE
Status
Cancelled Post Market
Status Date
2021-05-07
Original Market Date
2018-12-19
Din
02479494
Drug Class
Human
Dosage Form
Capsule
Route Of Administration
Oral
Schedule
Prescription
Ahfs
28:16.04.20
Atc Original
N06AB03 FLUOXETINE
Atc Name
n 06 ab 03
Aig Number
0116847001
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
FLUOXETINE (FLUOXETINE HYDROCHLORIDE)
20 MG
Authorized
Quick Info
Agency
Health Canada
Country
🇨🇦
Approval Date
Jul 4, 2025
Approval ID
ad613651e3224133
Type
Standard
Back to Health Canada Approvals