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VISTITAN DIN 02429063

Status: Marketed
Holder: SANDOZ CANADA INCORPORATED
Molecule: BIMATOPROST
Available to quote

Health Canada record

Active ingredient(s)BIMATOPROST 0.03 %
Dosage formSolution
RouteOphthalmic
SchedulePRESCRIPTION
ClassHuman
ATCS01EE03 BIMATOPROST
Original market date13-May-2016
Current status date13-May-2016
SourceHealth Canada DPD

Establishment licence of the holder

Sandoz Canada Incorporated — licence 101370, currently licensed, last inspection rating C (2025-02-25).

No Canadian shortage report is currently matched to this DIN.

Other Canadian products containing BIMATOPROST

DINProductCompanyFormStrengthStatus
02570068AG-BIMATOPROST RCANGITA PHARMA INC.SolutionBIMATOPROST 0.01 %Approved
02356279APO-BIMATOPROSTAPOTEX INCSolutionBIMATOPROST 0.03 %Approved
02402505APO-BIMATOPROSTAPOTEX INCSolutionBIMATOPROST 0.03 %Approved
02403013APO-BIMATOPROST RCAPOTEX INCSolutionBIMATOPROST 0.01 %Approved
02529580BIMATOPROST RCJUNO PHARMA CANADA INC.SolutionBIMATOPROST 0.01 %Marketed
02570904BIMATOPROST RCSANIS HEALTH INCSolutionBIMATOPROST 0.01 %Approved
02567385JAMP BIMATOPROSTJAMP PHARMA CORPORATIONSolutionBIMATOPROST 0.03 %Approved
02565773JAMP BIMATOPROST SOLUTION RCJAMP PHARMA CORPORATIONSolutionBIMATOPROST 0.01 %Marketed
02350939LATISSEABBVIE CORPORATIONSolutionBIMATOPROST 0.03 %Marketed
02324997LUMIGAN RCABBVIE CORPORATIONSolutionBIMATOPROST 0.01 %Marketed
02563428PRO-BIMATOPROST RCPRO DOC LIMITEESolutionBIMATOPROST 0.01 %Approved
02533464ZIMED PFLUVO MEDICAL TECHNOLOGIES INCSolutionBIMATOPROST 0.03 %Marketed
02245860LUMIGANALLERGAN INCSolutionBIMATOPROST 0.03 %Cancelled Post Market
02400162LUMIGAN PFALLERGAN INCSolutionBIMATOPROST 0.03 %Cancelled Pre Market
02425521SANDOZ BIMATOPROST RCSANDOZ CANADA INCORPORATEDSolutionBIMATOPROST 0.01 %Cancelled Pre Market

Notices of Compliance

NOCDateSubmissionReason
176162015-12-23Supplement to an Abbreviated New Drug Submission (SANDS)BRAND NAME CHANGE
158942014-08-01Abbreviated New Drug Submission (ANDS)

International API supply for BIMATOPROST

15 active FDA Drug Master Files.

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