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DULOXETINE - Health Canada Drug Approval Details
Approvals
/
Health Canada
/
DULOXETINE
Authorized
STANDARD
DULOXETINE
PRO DOC LIMITEE
🇨🇦 Health Canada
Approval Date
Jul 4, 2025
Approval ID
bffd19846e04e1ee
Company
PRO DOC LIMITEE
Type
Standard
Approval Details
Approval Id
bffd19846e04e1ee
Drug Approval Canada Name
DULOXETINE
Product Name
DULOXETINE
Status
Marketed
Status Date
2018-06-15
Original Market Date
2016-05-03
Din
02452669
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
PRO DOC LIMITEE
Company Address
2925 Boulevard Industriel, Laval, Quebec, Canada, H7L 3W9
Active Ingredients
DULOXETINE (DULOXETINE HYDROCHLORIDE)
60 MG
Authorized
Quick Info
Agency
Health Canada
Country
🇨🇦
Approval Date
Jul 4, 2025
Approval ID
bffd19846e04e1ee
Type
Standard
Back to Health Canada Approvals