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M-DULOXETINE - Health Canada Drug Approval Details
Approvals
/
Health Canada
/
M-DULOXETINE
Authorized
STANDARD
M-DULOXETINE
mantra pharma inc
🇨🇦 Health Canada
Approval Date
Jul 4, 2025
Approval ID
29c49e3b72dbf6c5
Company
mantra pharma inc
Type
Standard
Approval Details
Approval Id
29c49e3b72dbf6c5
Drug Approval Canada Name
M-DULOXETINE
Product Name
M-DULOXETINE
Status
Marketed
Status Date
2019-06-27
Original Market Date
2018-09-26
Din
02473216
Drug Class
Human
Dosage Form
Capsule (Delayed Release)
Route Of Administration
Oral
Schedule
Prescription
Ahfs
28:16.04.16
Atc Original
N06AX21 DULOXETINE
Atc Name
n 06 ax 21
Aig Number
0152350002
Company Name
mantra pharma inc
Company Address
1000 Rue Du Lux Suite 201, Brossard, Quebec, Canada, J4Y 0E3
Active Ingredients
DULOXETINE (DULOXETINE HYDROCHLORIDE)
60 MG
Authorized
Quick Info
Agency
Health Canada
Country
🇨🇦
Approval Date
Jul 4, 2025
Approval ID
29c49e3b72dbf6c5
Type
Standard
Back to Health Canada Approvals