PMS-DICLOFENAC K DIN 02239753
Health Canada record
| Active ingredient(s) | DICLOFENAC POTASSIUM 50 MG |
|---|---|
| Dosage form | Tablet |
| Route | Oral |
| Schedule | PRESCRIPTION |
| Class | Human |
| ATC | M01AB05 DICLOFENAC |
| Original market date | 04-Mar-1999 |
| Current status date | 18-May-2022 |
| Source | Health Canada DPD |
Establishment licence of the holder
Pharmascience Inc. — licence 100241, currently licensed, last inspection rating C (2025-03-20).
No Canadian shortage report is currently matched to this DIN.
Other Canadian products containing DICLOFENAC POTASSIUM
| DIN | Product | Company | Form | Strength | Status |
|---|---|---|---|---|---|
| 02567768 | APO-DICLOFENAC POWDER | APOTEX INC | Powder For Solution | DICLOFENAC POTASSIUM 50 MG | Approved |
| 02381680 | CAMBIA | ARALEZ PHARMACEUTICALS CANADA INC | Powder For Solution | DICLOFENAC POTASSIUM 50 MG | Marketed |
| 02563290 | JAMP DICLOFENAC FOR SOLUTION | JAMP PHARMA CORPORATION | Powder For Solution | DICLOFENAC POTASSIUM 50 MG | Marketed |
| 02560631 | RIVA-DICLOFENAC | LABORATOIRE RIVA INC. | Powder For Solution | DICLOFENAC POTASSIUM 50 MG | Marketed |
| 02261774 | SANDOZ DICLOFENAC RAPIDE | SANDOZ CANADA INCORPORATED | Tablet | DICLOFENAC POTASSIUM 50 MG | Marketed |
| 02564475 | TARO-DICLOFENAC POTASSIUM POWDER FOR ORAL SOLUTION | TARO PHARMACEUTICALS INC | Powder For Solution | DICLOFENAC POTASSIUM 50 MG | Marketed |
| 02239355 | TEVA-DICLOFENAC-K | TEVA CANADA LIMITED | Tablet | DICLOFENAC POTASSIUM 50 MG | Marketed |
| 00881635 | VOLTAREN RAPIDE | NOVARTIS PHARMACEUTICALS CANADA INC | Tablet | DICLOFENAC POTASSIUM 50 MG | Marketed |
| 02243433 | APO-DICLO RAPIDE 50 MG TABLETS | APOTEX INC | Tablet | DICLOFENAC POTASSIUM 50 MG | Cancelled Post Market |
| 02351684 | DICLOFENAC K | SANIS HEALTH INC | Tablet | DICLOFENAC POTASSIUM 50 MG | Cancelled Post Market |
| 02346281 | NTP-DICLOFENAC POTASSIUM | TEVA CANADA LIMITED | Tablet | DICLOFENAC POTASSIUM 50 MG | Cancelled Pre Market |
| 02336413 | NU-DICLO RAPIDE | NU-PHARM INC | Tablet | DICLOFENAC POTASSIUM 50 MG | Cancelled (Unreturned Annual) |
| 02311461 | PRO-DICLO RAPIDE - 50 | PRO DOC LIMITEE | Tablet | DICLOFENAC POTASSIUM 50 MG | Cancelled Post Market |
| 02240728 | RIVA-DICLOFENAC-K 50MG TABLETS | LABORATOIRE RIVA INC. | Tablet | DICLOFENAC POTASSIUM 50 MG | Cancelled Post Market |
Notices of Compliance
| NOC | Date | Submission | Reason |
|---|---|---|---|
| 1755 | 1999-03-04 | New Drug Submission (NDS) |
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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