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APO-ERLOTINIB DIN 02461889

Status: Marketed
Holder: APOTEX INC
Molecule: ERLOTINIB (ERLOTINIB HYDROCHLORIDE)
Available to quote

Health Canada record

Active ingredient(s)ERLOTINIB (ERLOTINIB HYDROCHLORIDE) 150 MG
Dosage formTablet
RouteOral
SchedulePRESCRIPTION
ClassHuman
ATCL01EB02 ERLOTINIB
Original market date22-Aug-2017
Current status date22-Aug-2017
SourceHealth Canada DPD

Establishment licence of the holder

Apotex Inc — licence 100375, currently licensed, last inspection rating C (2026-04-21).

No Canadian shortage report is currently matched to this DIN.

Other Canadian products containing ERLOTINIB (ERLOTINIB HYDROCHLORIDE)

DINProductCompanyFormStrengthStatus
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
02377705TEVA-ERLOTINIBTEVA CANADA LIMITEDTabletERLOTINIB (ERLOTINIB HYDROCHLORIDE) 100 MGMarketed
02377713TEVA-ERLOTINIBTEVA CANADA LIMITEDTabletERLOTINIB (ERLOTINIB HYDROCHLORIDE) 150 MGMarketed
02483912NAT-ERLOTINIBNATCO PHARMA (CANADA) INCTabletERLOTINIB (ERLOTINIB HYDROCHLORIDE) 25 MGDormant
02483920NAT-ERLOTINIBNATCO PHARMA (CANADA) INCTabletERLOTINIB (ERLOTINIB HYDROCHLORIDE) 100 MGDormant
02483939NAT-ERLOTINIBNATCO PHARMA (CANADA) INCTabletERLOTINIB (ERLOTINIB HYDROCHLORIDE) 150 MGDormant
02454386PMS-ERLOTINIBPHARMASCIENCE INCTabletERLOTINIB (ERLOTINIB HYDROCHLORIDE) 100 MGDormant
02269007TARCEVAHOFFMANN-LA ROCHE LIMITEDTabletERLOTINIB (ERLOTINIB HYDROCHLORIDE) 25 MGCancelled Post Market
02269023TARCEVAHOFFMANN-LA ROCHE LIMITEDTabletERLOTINIB (ERLOTINIB HYDROCHLORIDE) 150 MGCancelled Post Market
02269015TARCEVAHOFFMANN-LA ROCHE LIMITEDTabletERLOTINIB (ERLOTINIB HYDROCHLORIDE) 100 MGCancelled Post Market

Notices of Compliance

NOCDateSubmissionReason
190342017-03-09Abbreviated New Drug Submission (ANDS)
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