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VIIBRYD DIN 02443759

Status: Cancelled Post Market
Holder: ABBVIE CORPORATION
Molecule: VILAZODONE HYDROCHLORIDE

Health Canada record

Active ingredient(s)VILAZODONE HYDROCHLORIDE 10 MG; VILAZODONE HYDROCHLORIDE 20 MG
Dosage formKit; Tablet
RouteOral
SchedulePRESCRIPTION
ClassHuman
ATCN06AX24 VILAZODONE
Original market date06-Jul-2018
Current status date20-Jul-2023
SourceHealth Canada DPD

Establishment licence of the holder

AbbVie Corporation — licence 101988, currently licensed, last inspection rating C (2023-07-18).

No Canadian shortage report is currently matched to this DIN.

Other Canadian products containing VILAZODONE HYDROCHLORIDE

DINProductCompanyFormStrengthStatus
02551810APO-VILAZODONEAPOTEX INCTabletVILAZODONE HYDROCHLORIDE 10 MGMarketed
02551837APO-VILAZODONEAPOTEX INCTabletVILAZODONE HYDROCHLORIDE 40 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
02443732VIIBRYDABBVIE CORPORATIONTabletVILAZODONE HYDROCHLORIDE 20 MGMarketed
02443724VIIBRYDABBVIE CORPORATIONTabletVILAZODONE HYDROCHLORIDE 10 MGMarketed
02443740VIIBRYDABBVIE CORPORATIONTabletVILAZODONE HYDROCHLORIDE 40 MGMarketed
02443767VIIBRYDFOREST LABORATORIES CANADA INCKit; TabletVILAZODONE HYDROCHLORIDE 10 MG; VILAZODONE HYDROCHLORIDE 20 MG; VILAZODONE HYDROCHLORIDE 40 MGCancelled Pre Market

Notices of Compliance

NOCDateSubmissionReason
295132022-11-21New Drug Submission (NDS)Administrative: Merger/Buy-out
170962015-07-16New Drug Submission (NDS)

International API supply for VILAZODONE HYDROCHLORIDE

15 active FDA Drug Master Files.

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