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Q-PAROXETINE DIN 02338807

Status: Cancelled Post Market
Holder: QD PHARMACEUTICALS ULC
Molecule: PAROXETINE (PAROXETINE HYDROCHLORIDE, ISOPROPYL SOLVATE)

Health Canada record

Active ingredient(s)PAROXETINE (PAROXETINE HYDROCHLORIDE, ISOPROPYL SOLVATE) 20 MG
Dosage formTablet
RouteOral
SchedulePRESCRIPTION
ClassHuman
ATCN06AB05 PAROXETINE
Original market date24-Nov-2011
Current status date21-Aug-2015
SourceHealth Canada DPD

No Canadian shortage report is currently matched to this DIN.

Other Canadian products containing PAROXETINE (PAROXETINE HYDROCHLORIDE, ISOPROPYL SOLVATE)

DINProductCompanyFormStrengthStatus
02248014MYLAN-PAROXETINEMYLAN PHARMACEUTICALS ULCTabletPAROXETINE (PAROXETINE HYDROCHLORIDE, ISOPROPYL SOLVATE) 30 MGCancelled Post Market
02248012MYLAN-PAROXETINEMYLAN PHARMACEUTICALS ULCTabletPAROXETINE (PAROXETINE HYDROCHLORIDE, ISOPROPYL SOLVATE) 10 MGCancelled Post Market
02248013MYLAN-PAROXETINEMYLAN PHARMACEUTICALS ULCTabletPAROXETINE (PAROXETINE HYDROCHLORIDE, ISOPROPYL SOLVATE) 20 MGCancelled Post Market
02338793Q-PAROXETINEQD PHARMACEUTICALS ULCTabletPAROXETINE (PAROXETINE HYDROCHLORIDE, ISOPROPYL SOLVATE) 10 MGCancelled Post Market
02338815Q-PAROXETINEQD PHARMACEUTICALS ULCTabletPAROXETINE (PAROXETINE HYDROCHLORIDE, ISOPROPYL SOLVATE) 30 MGCancelled Post Market
02254751SANDOZ PAROXETINESANDOZ CANADA INCORPORATEDTabletPAROXETINE (PAROXETINE HYDROCHLORIDE, ISOPROPYL SOLVATE) 20 MGCancelled Post Market
02254778SANDOZ PAROXETINESANDOZ CANADA INCORPORATEDTabletPAROXETINE (PAROXETINE HYDROCHLORIDE, ISOPROPYL SOLVATE) 30 MGCancelled Post Market

Notices of Compliance

NOCDateSubmissionReason
127602011-11-04Abbreviated New Drug Submission (ANDS)Manufacturer Name Change
108502009-12-10Abbreviated New Drug Submission (ANDS)Additional product name
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