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APO-DESVENLAFAXINE EXTENDED-RELEASE TABLETS - Health Canada Drug Approval Details

Approvals/Health Canada/APO-DESVENLAFAXINE EXTENDED-RELEASE TABLETS

Authorized

STANDARD

APO-DESVENLAFAXINE EXTENDED-RELEASE TABLETS

Apotex Inc🇨🇦 Health Canada

Approval Date: Jul 4, 2025
Approval ID: f36ea4fb997b01be
Company: Apotex Inc
Type: Standard

Approval Details

Approval Id: f36ea4fb997b01be
Drug Approval Canada Name: APO-DESVENLAFAXINE EXTENDED-RELEASE TABLETS
Product Name: APO-DESVENLAFAXINE EXTENDED-RELEASE TABLETS
Status: Dormant
Status Date: 2025-04-19
Original Market Date: 2022-04-26
Din: 02467119
Drug Class: Human
Dosage Form: Tablet (Extended-Release)
Route Of Administration: Oral
Schedule: Prescription
Ahfs: 28:16.04.16
Atc Original: N06AX23 DESVENLAFAXINE
Atc Name: n 06 ax 23
Aig Number: 0152509001
Company Name: Apotex Inc
Company Address: 150 Signet Drive, Toronto, Ontario, Canada, M9L 1T9
Company Detail Path: /organization/apotex-inc

Company Information

Pharmaceutical Company Name: Apotex Inc
Country Name: Canada
Province Name: Ontario
City Name: toronto,ontario,country_ca
Address: 150 Signet Dr

Active Ingredients

DESVENLAFAXINE (DESVENLAFAXINE SUCCINATE)

50 MG

Authorized

Quick Info

Agency

Health Canada

Country

🇨🇦

Approval Date

Jul 4, 2025

Approval ID

f36ea4fb997b01be

Type

Standard

Back to Health Canada Approvals