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KEMADRIN TAB 5MG DIN 00004758

Status: Cancelled Post Market
Holder: GLAXOSMITHKLINE INC
Molecule: PROCYCLIDINE HYDROCHLORIDE

Health Canada record

Active ingredient(s)PROCYCLIDINE HYDROCHLORIDE 5 MG
Dosage formTablet
RouteOral
SchedulePRESCRIPTION
ClassHuman
ATCN04AA04 PROCYCLIDINE
Original market date31-Dec-1956
Current status date02-Dec-2004
SourceHealth Canada DPD

Establishment licence of the holder

GlaxoSmithKline Inc. — licence 100630, currently licensed, last inspection rating C (2025-09-15).

No Canadian shortage report is currently matched to this DIN.

Other Canadian products containing PROCYCLIDINE HYDROCHLORIDE

DINProductCompanyFormStrengthStatus
02427834PENDO-PROCYCLIDINEPENDOPHARM DIVISION OF PHARMASCIENCE INCTabletPROCYCLIDINE HYDROCHLORIDE 2.5 MGApproved
00004405KEMADRIN ELXGLAXOSMITHKLINE INCElixirPROCYCLIDINE HYDROCHLORIDE 2.5 MGCancelled Post Market
00649392PDP-PROCYCLIDINEPENDOPHARM DIVISION OF PHARMASCIENCE INCTabletPROCYCLIDINE HYDROCHLORIDE 2.5 MGDormant
00587354PDP-PROCYCLIDINEPENDOPHARM DIVISION OF PHARMASCIENCE INCTabletPROCYCLIDINE HYDROCHLORIDE 5 MGDormant
00587362PDP-PROCYCLIDINEPENDOPHARM DIVISION OF PHARMASCIENCE INCElixirPROCYCLIDINE HYDROCHLORIDE 2.5 MGDormant
02237042PHL-PROCYCLIDINE TABLETSPHARMEL INCTabletPROCYCLIDINE HYDROCHLORIDE 2.5 MGCancelled Post Market
02237043PHL-PROCYCLIDINE TABLETSPHARMEL INCTabletPROCYCLIDINE HYDROCHLORIDE 5 MGCancelled Post Market
00485012PROCYCLID ELXICN CANADA LTD.ElixirPROCYCLIDINE HYDROCHLORIDE 2.5 MGCancelled Post Market
00306290PROCYCLID TAB 5MGICN CANADA LTD.TabletPROCYCLIDINE HYDROCHLORIDE 5 MGCancelled Post Market

Notices of Compliance

NOCDateSubmissionReason
25032001-11-21New Drug Submission (NDS)CHANGE IN MANUFACTURER NAME

International API supply for PROCYCLIDINE HYDROCHLORIDE

0 active FDA Drug Master Files.

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