SANDOZ PAROXETINE DIN 02269449
Status: Cancelled Post Market
Holder: SANDOZ CANADA INCORPORATED
Molecule: PAROXETINE (PAROXETINE HYDROCHLORIDE)
Health Canada record
| Active ingredient(s) | PAROXETINE (PAROXETINE HYDROCHLORIDE) 30 MG |
|---|---|
| Dosage form | Tablet |
| Route | Oral |
| Schedule | PRESCRIPTION |
| Class | Human |
| ATC | N06AB05 PAROXETINE |
| Original market date | 27-Jul-2007 |
| Current status date | 01-Aug-2019 |
| Source | Health Canada DPD |
Establishment licence of the holder
Sandoz Canada Incorporated — licence 101370, currently licensed, last inspection rating C (2025-02-25).
No Canadian shortage report is currently matched to this DIN.
Other Canadian products containing PAROXETINE (PAROXETINE HYDROCHLORIDE)
| DIN | Product | Company | Form | Strength | Status |
|---|---|---|---|---|---|
| 02510480 | AG-PAROXETINE TABLETS | ANGITA PHARMA INC. | Tablet | PAROXETINE (PAROXETINE HYDROCHLORIDE) 10 MG | Marketed |
| 02510499 | AG-PAROXETINE TABLETS | ANGITA PHARMA INC. | Tablet | PAROXETINE (PAROXETINE HYDROCHLORIDE) 20 MG | Marketed |
| 02510510 | AG-PAROXETINE TABLETS | ANGITA PHARMA INC. | Tablet | PAROXETINE (PAROXETINE HYDROCHLORIDE) 30 MG | Marketed |
| 02240908 | APO-PAROXETINE | APOTEX INC | Tablet | PAROXETINE (PAROXETINE HYDROCHLORIDE) 20 MG | Marketed |
| 02240907 | APO-PAROXETINE | APOTEX INC | Tablet | PAROXETINE (PAROXETINE HYDROCHLORIDE) 10 MG | Marketed |
| 02240909 | APO-PAROXETINE | APOTEX INC | Tablet | PAROXETINE (PAROXETINE HYDROCHLORIDE) 30 MG | Marketed |
| 02507773 | JAMP PAROXETINE TABLETS | JAMP PHARMA CORPORATION | Tablet | PAROXETINE (PAROXETINE HYDROCHLORIDE) 10 MG | Marketed |
| 02507803 | JAMP PAROXETINE TABLETS | JAMP PHARMA CORPORATION | Tablet | PAROXETINE (PAROXETINE HYDROCHLORIDE) 30 MG | Marketed |
| 02507781 | JAMP PAROXETINE TABLETS | JAMP PHARMA CORPORATION | Tablet | PAROXETINE (PAROXETINE HYDROCHLORIDE) 20 MG | Marketed |
| 02388235 | PAROXETINE | SIVEM PHARMACEUTICALS ULC | Tablet | PAROXETINE (PAROXETINE HYDROCHLORIDE) 20 MG | Marketed |
| 02388227 | PAROXETINE | SIVEM PHARMACEUTICALS ULC | Tablet | PAROXETINE (PAROXETINE HYDROCHLORIDE) 10 MG | Marketed |
| 02388243 | PAROXETINE | SIVEM PHARMACEUTICALS ULC | Tablet | PAROXETINE (PAROXETINE HYDROCHLORIDE) 30 MG | Marketed |
| 02248504 | PAXIL CR | GLAXOSMITHKLINE INC | Tablet (Extended-Release) | PAROXETINE (PAROXETINE HYDROCHLORIDE) 25 MG | Marketed |
| 02248503 | PAXIL CR | GLAXOSMITHKLINE INC | Tablet (Extended-Release) | PAROXETINE (PAROXETINE HYDROCHLORIDE) 12.5 MG | Marketed |
| 01940481 | PAXIL TAB 20MG | GLAXOSMITHKLINE INC | Tablet | PAROXETINE (PAROXETINE HYDROCHLORIDE) 20 MG | Marketed |
| 02247752 | PMS-PAROXETINE | PHARMASCIENCE INC | Tablet | PAROXETINE (PAROXETINE HYDROCHLORIDE) 30 MG | Marketed |
| 02247751 | PMS-PAROXETINE | PHARMASCIENCE INC | Tablet | PAROXETINE (PAROXETINE HYDROCHLORIDE) 20 MG | Marketed |
| 02247750 | PMS-PAROXETINE | PHARMASCIENCE INC | Tablet | PAROXETINE (PAROXETINE HYDROCHLORIDE) 10 MG | Marketed |
| 02248914 | PRO-PAROXETINE | PRO DOC LIMITEE | Tablet | PAROXETINE (PAROXETINE HYDROCHLORIDE) 20 MG | Marketed |
| 02248915 | PRO-PAROXETINE | PRO DOC LIMITEE | Tablet | PAROXETINE (PAROXETINE HYDROCHLORIDE) 30 MG | Marketed |
| 02248913 | PRO-PAROXETINE | PRO DOC LIMITEE | Tablet | PAROXETINE (PAROXETINE HYDROCHLORIDE) 10 MG | Marketed |
| 02262754 | ACT PAROXETINE | ACTAVIS PHARMA COMPANY | Tablet | PAROXETINE (PAROXETINE HYDROCHLORIDE) 20 MG | Cancelled Post Market |
| 02262746 | ACT PAROXETINE | ACTAVIS PHARMA COMPANY | Tablet | PAROXETINE (PAROXETINE HYDROCHLORIDE) 10 MG | Cancelled Post Market |
| 02262762 | ACT PAROXETINE | ACTAVIS PHARMA COMPANY | Tablet | PAROXETINE (PAROXETINE HYDROCHLORIDE) 30 MG | Cancelled Post Market |
| 02298961 | DOM-PAROXETINE | DOMINION PHARMACAL | Tablet | PAROXETINE (PAROXETINE HYDROCHLORIDE) 40 MG | Cancelled Pre Market |
| 02248721 | NU-PAROXETINE | NU-PHARM INC | Tablet | PAROXETINE (PAROXETINE HYDROCHLORIDE) 30 MG | Cancelled (Unreturned Annual) |
| 02248719 | NU-PAROXETINE | NU-PHARM INC | Tablet | PAROXETINE (PAROXETINE HYDROCHLORIDE) 10 MG | Cancelled (Unreturned Annual) |
| 02248720 | NU-PAROXETINE | NU-PHARM INC | Tablet | PAROXETINE (PAROXETINE HYDROCHLORIDE) 20 MG | Cancelled (Unreturned Annual) |
| 02342391 | PAROXETINE | COBALT PHARMACEUTICALS COMPANY | Tablet | PAROXETINE (PAROXETINE HYDROCHLORIDE) 20 MG | Cancelled Pre Market |
| 02342405 | PAROXETINE | COBALT PHARMACEUTICALS COMPANY | Tablet | PAROXETINE (PAROXETINE HYDROCHLORIDE) 30 MG | Cancelled Pre Market |
| 02342383 | PAROXETINE | COBALT PHARMACEUTICALS COMPANY | Tablet | PAROXETINE (PAROXETINE HYDROCHLORIDE) 10 MG | Cancelled Pre Market |
| 02267128 | PAXIL CR | GLAXOSMITHKLINE INC | Tablet (Extended-Release) | PAROXETINE (PAROXETINE HYDROCHLORIDE) 37.5 MG | Cancelled Pre Market |
| 02027887 | PAXIL TAB 10MG | GLAXOSMITHKLINE INC | Tablet | PAROXETINE (PAROXETINE HYDROCHLORIDE) 10 MG | Cancelled Post Market |
| 01940473 | PAXIL TAB 30MG | GLAXOSMITHKLINE INC | Tablet | PAROXETINE (PAROXETINE HYDROCHLORIDE) 30 MG | Cancelled Post Market |
| 02293749 | PMS-PAROXETINE | PHARMASCIENCE INC | Tablet | PAROXETINE (PAROXETINE HYDROCHLORIDE) 40 MG | Dormant |
| 02247811 | RATIO-PAROXETINE | RATIOPHARM INC DIVISION OF TEVA CANADA LIMITED | Tablet | PAROXETINE (PAROXETINE HYDROCHLORIDE) 20 MG | Cancelled Post Market |
| 02247812 | RATIO-PAROXETINE | RATIOPHARM INC DIVISION OF TEVA CANADA LIMITED | Tablet | PAROXETINE (PAROXETINE HYDROCHLORIDE) 30 MG | Cancelled Post Market |
| 02247810 | RATIO-PAROXETINE | RATIOPHARM INC DIVISION OF TEVA CANADA LIMITED | Tablet | PAROXETINE (PAROXETINE HYDROCHLORIDE) 10 MG | Cancelled Post Market |
| 02269422 | SANDOZ PAROXETINE | SANDOZ CANADA INCORPORATED | Tablet | PAROXETINE (PAROXETINE HYDROCHLORIDE) 10 MG | Cancelled Post Market |
| 02269430 | SANDOZ PAROXETINE | SANDOZ CANADA INCORPORATED | Tablet | PAROXETINE (PAROXETINE HYDROCHLORIDE) 20 MG | Cancelled Post Market |
| 02431777 | SANDOZ PAROXETINE TABLETS | SANDOZ CANADA INCORPORATED | Tablet | PAROXETINE (PAROXETINE HYDROCHLORIDE) 10 MG | Cancelled Post Market |
| 02431793 | SANDOZ PAROXETINE TABLETS | SANDOZ CANADA INCORPORATED | Tablet | PAROXETINE (PAROXETINE HYDROCHLORIDE) 30 MG | Cancelled Post Market |
| 02431785 | SANDOZ PAROXETINE TABLETS | SANDOZ CANADA INCORPORATED | Tablet | PAROXETINE (PAROXETINE HYDROCHLORIDE) 20 MG | Cancelled Post Market |
Notices of Compliance
| NOC | Date | Submission | Reason |
|---|---|---|---|
| 8894 | 2007-07-06 | Abbreviated New Drug Submission (ANDS) |