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MYLAN-PAROXETINE DIN 02248013

Status: Cancelled Post Market
Holder: MYLAN 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 date08-Oct-2003
Current status date12-Jul-2018
SourceHealth Canada DPD

Establishment licence of the holder

Mylan Pharmaceuticals ULC — licence 101774, currently licensed, last inspection rating C (2026-02-24).

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
02338807Q-PAROXETINEQD PHARMACEUTICALS ULCTabletPAROXETINE (PAROXETINE HYDROCHLORIDE, ISOPROPYL SOLVATE) 20 MGCancelled Post Market
02338815Q-PAROXETINEQD PHARMACEUTICALS ULCTabletPAROXETINE (PAROXETINE HYDROCHLORIDE, ISOPROPYL SOLVATE) 30 MGCancelled Post Market
02338793Q-PAROXETINEQD PHARMACEUTICALS ULCTabletPAROXETINE (PAROXETINE HYDROCHLORIDE, ISOPROPYL SOLVATE) 10 MGCancelled Post Market
02254778SANDOZ PAROXETINESANDOZ CANADA INCORPORATEDTabletPAROXETINE (PAROXETINE HYDROCHLORIDE, ISOPROPYL SOLVATE) 30 MGCancelled Post Market
02254751SANDOZ PAROXETINESANDOZ CANADA INCORPORATEDTabletPAROXETINE (PAROXETINE HYDROCHLORIDE, ISOPROPYL SOLVATE) 20 MGCancelled Post Market

Notices of Compliance

NOCDateSubmissionReason
103512009-07-09Abbreviated New Drug Submission (ANDS)Manufacturer and product name change
34542003-10-08Abbreviated New Drug Submission (ANDS)
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