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LEVITRA DIN 02250470

Status: Cancelled Post Market
Holder: BAYER INC
Molecule: VARDENAFIL (VARDENAFIL HYDROCHLORIDE)

Health Canada record

Active ingredient(s)VARDENAFIL (VARDENAFIL HYDROCHLORIDE) 10 MG
Dosage formTablet
RouteOral
SchedulePRESCRIPTION
ClassHuman
ATCG04BE09 VARDENAFIL
Original market date17-Mar-2004
Current status date21-Dec-2022
SourceHealth Canada DPD

Establishment licence of the holder

Bayer Inc — licence 101029, currently licensed, last inspection rating C (2023-02-07).

No Canadian shortage report is currently matched to this DIN.

Other Canadian products containing VARDENAFIL (VARDENAFIL HYDROCHLORIDE)

DINProductCompanyFormStrengthStatus
02484587AG-VARDENAFILANGITA PHARMA INC.TabletVARDENAFIL (VARDENAFIL HYDROCHLORIDE) 5 MGApproved
02484609AG-VARDENAFILANGITA PHARMA INC.TabletVARDENAFIL (VARDENAFIL HYDROCHLORIDE) 20 MGApproved
02484595AG-VARDENAFILANGITA PHARMA INC.TabletVARDENAFIL (VARDENAFIL HYDROCHLORIDE) 10 MGApproved
02471647APO-VARDENAFILAPOTEX INCTabletVARDENAFIL (VARDENAFIL HYDROCHLORIDE) 5 MGMarketed
02471655APO-VARDENAFILAPOTEX INCTabletVARDENAFIL (VARDENAFIL HYDROCHLORIDE) 10 MGMarketed
02471663APO-VARDENAFILAPOTEX INCTabletVARDENAFIL (VARDENAFIL HYDROCHLORIDE) 20 MGMarketed
02475677JAMP-VARDENAFILJAMP PHARMA CORPORATIONTabletVARDENAFIL (VARDENAFIL HYDROCHLORIDE) 5 MGMarketed
02475685JAMP-VARDENAFILJAMP PHARMA CORPORATIONTabletVARDENAFIL (VARDENAFIL HYDROCHLORIDE) 10 MGMarketed
02475693JAMP-VARDENAFILJAMP PHARMA CORPORATIONTabletVARDENAFIL (VARDENAFIL HYDROCHLORIDE) 20 MGMarketed
02250462LEVITRABAYER INCTabletVARDENAFIL (VARDENAFIL HYDROCHLORIDE) 5 MGCancelled Post Market
02250489LEVITRABAYER INCTabletVARDENAFIL (VARDENAFIL HYDROCHLORIDE) 20 MGCancelled Post Market
02372436STAXYNBAYER INCTablet (Orally-Disintegrating)VARDENAFIL (VARDENAFIL HYDROCHLORIDE) 10 MGCancelled Post Market

Notices of Compliance

NOCDateSubmissionReason
1832004-03-17New Drug Submission (NDS)
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