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PROPOFOL-II INJECTION DIN 02376865

Status: Cancelled Post Market
Holder: PFIZER CANADA ULC
Molecule: PROPOFOL

Health Canada record

Active ingredient(s)PROPOFOL 10 MG
Dosage formEmulsion
RouteIntravenous
SchedulePRESCRIPTION
ClassHuman
ATCN01AX10 PROPOFOL
Original market date11-Jun-2013
Current status date24-Feb-2020
SourceHealth Canada DPD

Establishment licence of the holder

Pfizer Canada ULC — licence 100255, currently licensed, last inspection rating C (2023-08-07).

No Canadian shortage report is currently matched to this DIN.

Other Canadian products containing PROPOFOL

DINProductCompanyFormStrengthStatus
02018950DIPRIVAN 1%ASPEN PHARMACARE CANADA INC.EmulsionPROPOFOL 10 MGMarketed
02445654PROPOFLO 28ZOETIS CANADA INCSolutionPROPOFOL 10 MGMarketed
02559692PROPOFOL INJECTIONSTERIMAX INCEmulsionPROPOFOL 10 MGApproved
02244379PROPOFOL INJECTIONBAXTER CORPORATIONEmulsionPROPOFOL 10 MGMarketed
02437643PROPOFOL INJECTIONFRESENIUS KABI CANADA LTDEmulsionPROPOFOL 10 MGMarketed
02525879PROPOFOL INJECTIONMARCAN PHARMACEUTICALS INCEmulsionPROPOFOL 10 MGMarketed
02244685PROPOFLOABBOTT LABORATORIESEmulsionPROPOFOL 10 MGCancelled Post Market
02468336PROPOFOLBAXTER CORPORATIONEmulsionPROPOFOL 10 MGCancelled Post Market
02236887PROPOFOL INJECTIONPFIZER CANADA ULCEmulsionPROPOFOL 10 MGCancelled Post Market
02241504PROPOFOL INJECTIONNOVOPHARM LIMITEDEmulsionPROPOFOL 10 MGCancelled Post Market
02242973PROPOFOL INJECTIONHOSPIRA HEALTHCARE ULCEmulsionPROPOFOL 10 MGCancelled Post Market
02138255RAPINOVETINTERVET CANADA CORPSolutionPROPOFOL 10 MGCancelled Post Market
02437961TEVA-PROPOFOLTEVA CANADA LIMITEDEmulsionPROPOFOL 10 MGDormant

Notices of Compliance

NOCDateSubmissionReason
213812018-10-02Abbreviated New Drug Submission (ANDS)MERGER - BUYOUT
128102011-11-30Supplement to an Abbreviated New Drug Submission (SANDS)New Formulation

International API supply for PROPOFOL

8 valid EDQM Certificates of Suitability from 8 holders. 9 active FDA Drug Master Files.

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