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VEPESID DIN 00616192

Status: Marketed
Holder: CHEPLAPHARM ARZNEIMITTEL GMBH
Molecule: ETOPOSIDE
Available to quote

Health Canada record

Active ingredient(s)ETOPOSIDE 50 MG
Dosage formCapsule
RouteOral
SchedulePRESCRIPTION
ClassHuman
ATCL01CB01 ETOPOSIDE
Original market date31-Dec-1984
Current status date02-Jan-2020
SourceHealth Canada DPD

Establishment licence of the holder

Cheplapharm Arzneimittel GmbH — licence , not currently licensed, last inspection rating C (2024-10-10).

No Canadian shortage report is currently matched to this DIN.

Other Canadian products containing ETOPOSIDE

DINProductCompanyFormStrengthStatus
02080036ETOPOSIDE INJECTIONTEVA CANADA LIMITEDSolutionETOPOSIDE 20 MGMarketed
02552671ETOPOSIDE INJECTIONHIKMA CANADA LIMITEDSolutionETOPOSIDE 20 MGMarketed
02237872DOM-ETOPOSIDEDOMINION PHARMACALLiquidETOPOSIDE 20 MGCancelled Pre Market
02237428EPOSINPHARMACHEMIE B.V.LiquidETOPOSIDE 20 MGCancelled Pre Market
02237873ETOPOSIDEPHARMEL INCLiquidETOPOSIDE 20 MGCancelled Pre Market
02227509ETOPOSIDE - LIQ IV 20MG/MLBDH INC.LiquidETOPOSIDE 20 MGCancelled Post Market
02239961ETOPOSIDE INJECTIONFRESENIUS KABI CANADA LTDLiquidETOPOSIDE 20 MGDormant
02380935ETOPOSIDE INJECTION USPSANDOZ CANADA INCORPORATEDSolutionETOPOSIDE 20 MGCancelled Post Market
02241182ETOPOSIDE INJECTION, USPHOSPIRA HEALTHCARE ULCSolutionETOPOSIDE 20 MGCancelled Post Market
02422530ETOPOSIDE INJECTION, USPSTRIDES PHARMA CANADA INCSolutionETOPOSIDE 20 MGDormant
02237871PMS-ETOPOSIDEPHARMASCIENCE INCLiquidETOPOSIDE 20 MGCancelled Pre Market
00523410VEPESID INJ 20MG/MLBRISTOL LABS DIVISION OF BRISTOL-MYERS SQUIBBLiquidETOPOSIDE 20 MGCancelled Post Market

Notices of Compliance

NOCDateSubmissionReason
230432019-12-19New Drug Submission (NDS)CHANGE IN PRODUCT OWNERSHIP
97092008-08-12New Drug Submission (NDS)MANUFACTURER NAME CHANGE

International API supply for ETOPOSIDE

6 valid EDQM Certificates of Suitability from 6 holders. 7 active FDA Drug Master Files.

Special Access Programme

This molecule appears on Health Canada's list of drugs most often requested through the Special Access Programme.

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