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QOSEQU DIN 02570750

Status: Approved
Holder: MANTRA PHARMA INC
Molecule: DENOSUMAB

Health Canada record

Active ingredient(s)DENOSUMAB 60 MG
Dosage formSolution
RouteSubcutaneous
ScheduleSCHEDULE D; PRESCRIPTION
ClassHuman
ATCM05BX04 DENOSUMAB
Original market date
Current status date12-Aug-2026
SourceHealth Canada DPD

Establishment licence of the holder

Mantra Pharma Inc. — licence 101740, currently licensed, last inspection rating C (2023-05-10).

No Canadian shortage report is currently matched to this DIN.

Other Canadian products containing DENOSUMAB

DINProductCompanyFormStrengthStatus
02565951BILDYOSSHANGHAI HENLIUS BIOTECH, INC.SolutionDENOSUMAB 60 MGMarketed
02565943BILDYOSSHANGHAI HENLIUS BIOTECH, INC.SolutionDENOSUMAB 60 MGApproved
02567679BOMYNTRAFRESENIUS KABI CANADA LTDSolutionDENOSUMAB 120 MGApproved
02567687BOMYNTRAFRESENIUS KABI CANADA LTDSolutionDENOSUMAB 120 MGApproved
02567253BOSAYABIOCON BIOLOGICS CANADA INCSolutionDENOSUMAB 60 MGApproved
02567660CONEXXENCEFRESENIUS KABI CANADA LTDSolutionDENOSUMAB 60 MGApproved
02566265DENOZAAPOTEX INCSolutionDENOSUMAB 60 MGMarketed
02566273IDENOSAPOTEX INCSolutionDENOSUMAB 120 MGApproved
02545411JUBBONTISANDOZ CANADA INCORPORATEDSolutionDENOSUMAB 60 MGMarketed
02567482OBODENCESAMSUNG BIOEPIS CO., LTDSolutionDENOSUMAB 60 MGApproved
02569787ODENSIFYJAMP PHARMA CORPORATIONSolutionDENOSUMAB 60 MGApproved
02560895OSENVELTCELLTRION INC.SolutionDENOSUMAB 120 MGMarketed
02343541PROLIAAMGEN CANADA INCSolutionDENOSUMAB 60 MGMarketed
02560917STOBOCLOCELLTRION INC.SolutionDENOSUMAB 60 MGMarketed
02566001TUZEMTYSHANGHAI HENLIUS BIOTECH, INC.SolutionDENOSUMAB 120 MGMarketed
02567261VEVZUOBIOCON BIOLOGICS CANADA INCSolutionDENOSUMAB 120 MGApproved
02545764WYOSTSANDOZ CANADA INCORPORATEDSolutionDENOSUMAB 120 MGMarketed
02566923XBRYKSAMSUNG BIOEPIS CO., LTDSolutionDENOSUMAB 120 MGApproved
02569795XDENOJAMP PHARMA CORPORATIONSolutionDENOSUMAB 120 MGApproved
02368153XGEVAAMGEN CANADA INCSolutionDENOSUMAB 120 MGMarketed
02343568PROLIAAMGEN CANADA INCSolutionDENOSUMAB 60 MGCancelled Pre Market

Notices of Compliance

NOCDateSubmissionReason
381002026-08-12New Drug Submission (NDS)
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