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Approvals
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Health Canada
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M-FLUOXETINE
Authorized
STANDARD
M-FLUOXETINE
mantra pharma inc
🇨🇦 Health Canada
Approval Date
Jul 4, 2025
Approval ID
e2927c61f10d3d6d
Company
mantra pharma inc
Type
Standard
Approval Details
Approval Id
e2927c61f10d3d6d
Drug Approval Canada Name
M-FLUOXETINE
Product Name
M-FLUOXETINE
Status
Marketed
Status Date
2024-10-17
Original Market Date
2023-03-17
Din
02529440
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
mantra pharma inc
Company Address
1000 Rue Du Lux Suite 201, Brossard, Quebec, Canada, J4Y 0E3
Active Ingredients
FLUOXETINE (FLUOXETINE HYDROCHLORIDE)
20 MG
Authorized
Quick Info
Agency
Health Canada
Country
🇨🇦
Approval Date
Jul 4, 2025
Approval ID
e2927c61f10d3d6d
Type
Standard
Back to Health Canada Approvals
M-FLUOXETINE - Health Canada Drug Approval Details