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APO-VILAZODONE DIN 02551837

Status: Marketed
Holder: APOTEX INC
Molecule: VILAZODONE HYDROCHLORIDE
Available to quote

Health Canada record

Active ingredient(s)VILAZODONE HYDROCHLORIDE 40 MG
Dosage formTablet
RouteOral
SchedulePRESCRIPTION
ClassHuman
ATCN06AX24 VILAZODONE
Original market date21-Feb-2025
Current status date21-Feb-2025
SourceHealth Canada DPD

Establishment licence of the holder

Apotex Inc — licence 100375, currently licensed, last inspection rating C (2026-04-21).

No Canadian shortage report is currently matched to this DIN.

Other Canadian products containing VILAZODONE HYDROCHLORIDE

DINProductCompanyFormStrengthStatus
02551810APO-VILAZODONEAPOTEX INCTabletVILAZODONE HYDROCHLORIDE 10 MGMarketed
02551829APO-VILAZODONEAPOTEX INCTabletVILAZODONE HYDROCHLORIDE 20 MGMarketed
02568705PMS-VILAZODONEPHARMASCIENCE INCTabletVILAZODONE HYDROCHLORIDE 40 MGApproved
02568683PMS-VILAZODONEPHARMASCIENCE INCTabletVILAZODONE HYDROCHLORIDE 10 MGApproved
02568691PMS-VILAZODONEPHARMASCIENCE INCTabletVILAZODONE HYDROCHLORIDE 20 MGApproved
02443740VIIBRYDABBVIE CORPORATIONTabletVILAZODONE HYDROCHLORIDE 40 MGMarketed
02443732VIIBRYDABBVIE CORPORATIONTabletVILAZODONE HYDROCHLORIDE 20 MGMarketed
02443724VIIBRYDABBVIE CORPORATIONTabletVILAZODONE HYDROCHLORIDE 10 MGMarketed
02443759VIIBRYDABBVIE CORPORATIONKit; TabletVILAZODONE HYDROCHLORIDE 10 MG; VILAZODONE HYDROCHLORIDE 20 MGCancelled Post Market
02443767VIIBRYDFOREST LABORATORIES CANADA INCKit; TabletVILAZODONE HYDROCHLORIDE 10 MG; VILAZODONE HYDROCHLORIDE 20 MG; VILAZODONE HYDROCHLORIDE 40 MGCancelled Pre Market

Notices of Compliance

NOCDateSubmissionReason
340302024-09-17Abbreviated New Drug Submission (ANDS)

International API supply for VILAZODONE HYDROCHLORIDE

15 active FDA Drug Master Files.

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