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DULOXETINE - Health Canada Drug Approval Details
Approvals
/
Health Canada
/
DULOXETINE
Authorized
STANDARD
DULOXETINE
altamed pharma
🇨🇦 Health Canada
Approval Date
Jul 4, 2025
Approval ID
c7672363440dd7fb
Company
altamed pharma
Type
Standard
Approval Details
Approval Id
c7672363440dd7fb
Drug Approval Canada Name
DULOXETINE
Product Name
DULOXETINE
Status
Marketed
Status Date
2023-10-05
Original Market Date
2023-10-05
Din
02481952
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
0152350001
Company Name
altamed pharma
Company Address
151 Boulevard De Mortagne, Boucherville, Quebec, Canada, J4B 6G4
Active Ingredients
DULOXETINE (DULOXETINE HYDROCHLORIDE)
30 MG
Authorized
Quick Info
Agency
Health Canada
Country
🇨🇦
Approval Date
Jul 4, 2025
Approval ID
c7672363440dd7fb
Type
Standard
Back to Health Canada Approvals