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TEVA-ERLOTINIB DIN 02377705

Status: Marketed
Holder: TEVA CANADA LIMITED
Molecule: ERLOTINIB (ERLOTINIB HYDROCHLORIDE)
Available to quote

Health Canada record

Active ingredient(s)ERLOTINIB (ERLOTINIB HYDROCHLORIDE) 100 MG
Dosage formTablet
RouteOral
SchedulePRESCRIPTION
ClassHuman
ATCL01EB02 ERLOTINIB
Original market date08-Dec-2014
Current status date08-Dec-2014
SourceHealth Canada DPD

Establishment licence of the holder

Teva Canada Limited — licence 101810, currently licensed, last inspection rating C (2025-03-04).

No Canadian shortage report is currently matched to this DIN.

Other Canadian products containing ERLOTINIB (ERLOTINIB HYDROCHLORIDE)

DINProductCompanyFormStrengthStatus
02461889APO-ERLOTINIBAPOTEX INCTabletERLOTINIB (ERLOTINIB HYDROCHLORIDE) 150 MGMarketed
02461870APO-ERLOTINIBAPOTEX INCTabletERLOTINIB (ERLOTINIB HYDROCHLORIDE) 100 MGMarketed
02461862APO-ERLOTINIBAPOTEX INCTabletERLOTINIB (ERLOTINIB HYDROCHLORIDE) 25 MGMarketed
02454394PMS-ERLOTINIBPHARMASCIENCE INCTabletERLOTINIB (ERLOTINIB HYDROCHLORIDE) 150 MGMarketed
02377691TEVA-ERLOTINIBTEVA CANADA LIMITEDTabletERLOTINIB (ERLOTINIB HYDROCHLORIDE) 25 MGMarketed
02377713TEVA-ERLOTINIBTEVA CANADA LIMITEDTabletERLOTINIB (ERLOTINIB HYDROCHLORIDE) 150 MGMarketed
02483939NAT-ERLOTINIBNATCO PHARMA (CANADA) INCTabletERLOTINIB (ERLOTINIB HYDROCHLORIDE) 150 MGDormant
02483912NAT-ERLOTINIBNATCO PHARMA (CANADA) INCTabletERLOTINIB (ERLOTINIB HYDROCHLORIDE) 25 MGDormant
02483920NAT-ERLOTINIBNATCO PHARMA (CANADA) INCTabletERLOTINIB (ERLOTINIB HYDROCHLORIDE) 100 MGDormant
02454386PMS-ERLOTINIBPHARMASCIENCE INCTabletERLOTINIB (ERLOTINIB HYDROCHLORIDE) 100 MGDormant
02269015TARCEVAHOFFMANN-LA ROCHE LIMITEDTabletERLOTINIB (ERLOTINIB HYDROCHLORIDE) 100 MGCancelled Post Market
02269007TARCEVAHOFFMANN-LA ROCHE LIMITEDTabletERLOTINIB (ERLOTINIB HYDROCHLORIDE) 25 MGCancelled Post Market
02269023TARCEVAHOFFMANN-LA ROCHE LIMITEDTabletERLOTINIB (ERLOTINIB HYDROCHLORIDE) 150 MGCancelled Post Market

Notices of Compliance

NOCDateSubmissionReason
164162014-12-08Abbreviated New Drug Submission (ANDS)
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