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RIVA-DICLOFENAC DIN 02560631

Status: Marketed
Holder: LABORATOIRE RIVA INC.
Molecule: DICLOFENAC POTASSIUM

Health Canada record

Active ingredient(s)DICLOFENAC POTASSIUM 50 MG
Dosage formPowder For Solution
RouteOral
SchedulePRESCRIPTION
ClassHuman
ATCM01AB05 DICLOFENAC
Original market date29-May-2026
Current status date29-May-2026
SourceHealth Canada DPD

Establishment licence of the holder

Laboratoire Riva Inc. — licence 100179, currently licensed, last inspection rating C (2026-01-12).

No Canadian shortage report is currently matched to this DIN.

Other Canadian products containing DICLOFENAC POTASSIUM

DINProductCompanyFormStrengthStatus
02567768APO-DICLOFENAC POWDERAPOTEX INCPowder For SolutionDICLOFENAC POTASSIUM 50 MGApproved
02381680CAMBIAARALEZ PHARMACEUTICALS CANADA INCPowder For SolutionDICLOFENAC POTASSIUM 50 MGMarketed
02563290JAMP DICLOFENAC FOR SOLUTIONJAMP PHARMA CORPORATIONPowder For SolutionDICLOFENAC POTASSIUM 50 MGMarketed
02261774SANDOZ DICLOFENAC RAPIDESANDOZ CANADA INCORPORATEDTabletDICLOFENAC POTASSIUM 50 MGMarketed
02564475TARO-DICLOFENAC POTASSIUM POWDER FOR ORAL SOLUTIONTARO PHARMACEUTICALS INCPowder For SolutionDICLOFENAC POTASSIUM 50 MGMarketed
02239355TEVA-DICLOFENAC-KTEVA CANADA LIMITEDTabletDICLOFENAC POTASSIUM 50 MGMarketed
00881635VOLTAREN RAPIDENOVARTIS PHARMACEUTICALS CANADA INCTabletDICLOFENAC POTASSIUM 50 MGMarketed
02243433APO-DICLO RAPIDE 50 MG TABLETSAPOTEX INCTabletDICLOFENAC POTASSIUM 50 MGCancelled Post Market
02351684DICLOFENAC KSANIS HEALTH INCTabletDICLOFENAC POTASSIUM 50 MGCancelled Post Market
02346281NTP-DICLOFENAC POTASSIUMTEVA CANADA LIMITEDTabletDICLOFENAC POTASSIUM 50 MGCancelled Pre Market
02336413NU-DICLO RAPIDENU-PHARM INCTabletDICLOFENAC POTASSIUM 50 MGCancelled (Unreturned Annual)
02239753PMS-DICLOFENAC KPHARMASCIENCE INCTabletDICLOFENAC POTASSIUM 50 MGCancelled Post Market
02311461PRO-DICLO RAPIDE - 50PRO DOC LIMITEETabletDICLOFENAC POTASSIUM 50 MGCancelled Post Market
02240728RIVA-DICLOFENAC-K 50MG TABLETSLABORATOIRE RIVA INC.TabletDICLOFENAC POTASSIUM 50 MGCancelled Post Market

Notices of Compliance

NOCDateSubmissionReason
374132026-04-28Abbreviated New Drug Submission (ANDS)

International API supply for DICLOFENAC POTASSIUM

4 valid EDQM Certificates of Suitability from 4 holders. 7 active FDA Drug Master Files.

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