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RATIO-SULFASALAZINE EN DIN 00685925

Status: Cancelled Post Market
Holder: RATIOPHARM INC DIVISION OF TEVA CANADA LIMITED
Molecule: SULFASALAZINE

Health Canada record

Active ingredient(s)SULFASALAZINE 500 MG
Dosage formTablet (Enteric-Coated)
RouteOral
SchedulePRESCRIPTION
ClassHuman
ATCA07EC01 SULFASALAZINE
Original market date31-Dec-1986
Current status date01-Aug-2008
SourceHealth Canada DPD

No Canadian shortage report is currently matched to this DIN.

Other Canadian products containing SULFASALAZINE

DINProductCompanyFormStrengthStatus
02544652JAMP SULFASALAZINEJAMP PHARMA CORPORATIONTabletSULFASALAZINE 500 MGMarketed
00598461PMS-SULFASALAZINE 500MG/TAB USPPHARMASCIENCE INCTabletSULFASALAZINE 500 MGMarketed
00598488PMS-SULFASALAZINE-E.C. TAB 500MGPHARMASCIENCE INCTablet (Enteric-Coated)SULFASALAZINE 500 MGMarketed
02064472SALAZOPYRIN EN-TABS 500 MGPFIZER CANADA ULCTablet (Enteric-Coated)SULFASALAZINE 500 MGMarketed
02064480SALAZOPYRIN TAB 500MGPFIZER CANADA ULCTabletSULFASALAZINE 500 MGMarketed
00410640APO SULFASALAZINE TAB 500MGAPOTEX INCTabletSULFASALAZINE 500 MGCancelled Post Market
02246803ORB-SULFASALAZINE ECORBUS PHARMA INCTablet (Enteric-Coated)SULFASALAZINE 500 MGCancelled (Unreturned Annual)
00685933RATIO-SULFASALAZINE TAB 500MGRATIOPHARM INC DIVISION OF TEVA CANADA LIMITEDTabletSULFASALAZINE 500 MGCancelled Post Market
00445126S.A.S. ENTERIC 500MGICN CANADA LTD.Tablet (Enteric-Coated)SULFASALAZINE 500 MGCancelled Post Market
02004682SALAZOPYRIN ENEMA 3.0GM/100MLKABI PHARMACIA CANADA INC.SuspensionSULFASALAZINE 3 GCancelled Post Market
02064499SALAZOPYRIN ENEMA 3GM/100MLPFIZER CANADA ULCEnemaSULFASALAZINE 3 GCancelled Post Market
00613568SAS ENEMA 3GM/100MLICN CANADA LTD.EnemaSULFASALAZINE 3 GCancelled Post Market
00263869SAS TAB 500MGICN CANADA LTD.TabletSULFASALAZINE 500 MGCancelled Post Market

Notices of Compliance

NOCDateSubmissionReason
9072002-05-08New Drug Submission (NDS)MANUFACTURER AND PRODUCT NAME CHANGE
46561996-10-08New Drug Submission (NDS)

International API supply for SULFASALAZINE

3 valid EDQM Certificates of Suitability from 3 holders. 4 active FDA Drug Master Files.

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