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M-DIENOGEST DIN 02543613

Status: Marketed
Holder: MANTRA PHARMA INC
Molecule: DIENOGEST
Available to quote

Health Canada record

Active ingredient(s)DIENOGEST 2 MG
Dosage formTablet
RouteOral
SchedulePRESCRIPTION
ClassHuman
ATCG03DB08 DIENOGEST
Original market date23-Apr-2024
Current status date23-Apr-2024
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 DIENOGEST

DINProductCompanyFormStrengthStatus
02493055ASPEN-DIENOGESTASPEN PHARMACARE CANADA INC.TabletDIENOGEST 2 MGMarketed
02567245BIO-DIENOGESTBIOMED PHARMATabletDIENOGEST 2 MGApproved
02569205DIENOGESTSANIS HEALTH INCTabletDIENOGEST 2 MGApproved
02498189JAMP DIENOGESTJAMP PHARMA CORPORATIONTabletDIENOGEST 2 MGMarketed
02551683MAR-DIENOGESTMARCAN PHARMACEUTICALS INCTabletDIENOGEST 2 MGMarketed
02566117NRA-DIENOGESTNORA PHARMA INCTabletDIENOGEST 2 MGApproved
02374900VISANNEBAYER INCTabletDIENOGEST 2 MGMarketed

Notices of Compliance

NOCDateSubmissionReason
322432023-12-01Abbreviated New Drug Submission (ANDS)

International API supply for DIENOGEST

2 valid EDQM Certificates of Suitability from 2 holders. 7 active FDA Drug Master Files.

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