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DESLORATADINE TABLETS DIN 02338424

Status: Dormant
Holder: APOTEX INC
Molecule: DESLORATADINE

Health Canada record

Active ingredient(s)DESLORATADINE 5 MG
Dosage formTablet
RouteOral
ScheduleNON-PRESCRIPTION DRUGS
ClassHuman
ATCR06AX27 DESLORATADINE
Original market date27-May-2010
Current status date04-Aug-2017
SourceHealth Canada DPD

Establishment licence of the holder

Apotex Inc — licence 100375, currently licensed, last inspection rating C (2026-04-21).

No Canadian shortage report is currently matched to this DIN.

Other Canadian products containing DESLORATADINE

DINProductCompanyFormStrengthStatus
02247192AERIUSBAYER INCSyrupDESLORATADINE 0.5 MGApproved
02243919AERIUSBAYER INCTabletDESLORATADINE 5 MGMarketed
02247193AERIUS KIDSBAYER INCSyrupDESLORATADINE 0.5 MGMarketed
02309300AERIUS SINUS + ALLERGYBAYER INCTablet (Extended-Release)DESLORATADINE 2.5 MG; PSEUDOEPHEDRINE SULFATE 120 MGMarketed
02415771ALLERGY CONTROL DESLORATADINEPHARMASCIENCE INCTabletDESLORATADINE 5 MGApproved
02546019DESLORATADINEJAMP PHARMA CORPORATIONTabletDESLORATADINE 5 MGMarketed
02298155DESLORATADINE ALLERGY CONTROLPHARMASCIENCE INCTabletDESLORATADINE 5 MGMarketed
02377195AERIUS DUAL ACTION 24 HOURBAYER INCTablet (Immediate- And Extended-Release)DESLORATADINE 5 MG; PSEUDOEPHEDRINE SULFATE 240 MGCancelled Pre Market
02369656ALLERNIX MULTI SYMPTOMTEVA CANADA LIMITEDTabletDESLORATADINE 5 MGCancelled Post Market
02408740DESLORATADINE ALLERGY CONTROLDOMINION PHARMACALTabletDESLORATADINE 5 MGCancelled Post Market

Notices of Compliance

NOCDateSubmissionReason
110122010-02-05Abbreviated New Drug Submission (ANDS)

International API supply for DESLORATADINE

11 valid EDQM Certificates of Suitability from 11 holders. 11 active FDA Drug Master Files.

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