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AG-DULOXETINE - Health Canada Drug Approval Details

Approvals/Health Canada/AG-DULOXETINE

Authorized

STANDARD

AG-DULOXETINE

angita pharma inc.🇨🇦 Health Canada

Approval Date: Jul 4, 2025
Approval ID: 05f12a4bb1789618
Company: angita pharma inc.
Type: Standard

Approval Details

Approval Id: 05f12a4bb1789618
Drug Approval Canada Name: AG-DULOXETINE
Product Name: AG-DULOXETINE
Status: Marketed
Status Date: 2018-07-19
Original Market Date: 2018-07-19
Din: 02475316
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: angita pharma inc.
Company Address: 1310 Rue Nobel, Boucherville, Quebec, Canada, J4B 5H3

Active Ingredients

DULOXETINE (DULOXETINE HYDROCHLORIDE)

60 MG

Authorized

Quick Info

Agency

Health Canada

Country

🇨🇦

Approval Date

Jul 4, 2025

Approval ID

05f12a4bb1789618

Type

Standard

Back to Health Canada Approvals