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INVEGA DIN 02300311

Status: Cancelled Pre Market
Holder: JANSSEN INC
Molecule: PALIPERIDONE

Health Canada record

Active ingredient(s)PALIPERIDONE 12 MG
Dosage formTablet (Extended-Release)
RouteOral
SchedulePRESCRIPTION
ClassHuman
ATCN05AX13 PALIPERIDONE
Original market date
Current status date30-Jul-2018
SourceHealth Canada DPD

Establishment licence of the holder

Janssen Inc — licence 100239, currently licensed, last inspection rating C (2026-03-09).

No Canadian shortage report is currently matched to this DIN.

Other Canadian products containing PALIPERIDONE

DINProductCompanyFormStrengthStatus
02300273INVEGAJANSSEN INCTablet (Extended-Release)PALIPERIDONE 3 MGMarketed
02300281INVEGAJANSSEN INCTablet (Extended-Release)PALIPERIDONE 6 MGMarketed
02300303INVEGAJANSSEN INCTablet (Extended-Release)PALIPERIDONE 9 MGMarketed
02511037MAR-PALIPERIDONEMARCAN PHARMACEUTICALS INCTablet (Extended-Release)PALIPERIDONE 9 MGCancelled Pre Market
02511010MAR-PALIPERIDONEMARCAN PHARMACEUTICALS INCTablet (Extended-Release)PALIPERIDONE 3 MGCancelled Post Market
02511029MAR-PALIPERIDONEMARCAN PHARMACEUTICALS INCTablet (Extended-Release)PALIPERIDONE 6 MGCancelled Post Market
02456400MYLAN-PALIPERIDONEMYLAN PHARMACEUTICALS ULCTablet (Extended-Release)PALIPERIDONE 3 MGCancelled Pre Market
02437139MYLAN-PALIPERIDONEMYLAN PHARMACEUTICALS ULCTablet (Extended-Release)PALIPERIDONE 6 MGCancelled Pre Market

Notices of Compliance

NOCDateSubmissionReason
90562007-09-26New Drug Submission (NDS)

International API supply for PALIPERIDONE

40 active FDA Drug Master Files.

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