ELOXATIN DIN 02296284
Health Canada record
| Active ingredient(s) | OXALIPLATIN 5 MG |
|---|---|
| Dosage form | Solution |
| Route | Intravenous |
| Schedule | PRESCRIPTION |
| Class | Human |
| ATC | L01XA03 OXALIPLATIN |
| Original market date | 17-Jul-2007 |
| Current status date | 09-Nov-2018 |
| Source | Health Canada DPD |
Establishment licence of the holder
sanofi-aventis Canada Inc. — licence 101470, currently licensed, last inspection rating C (2026-02-17).
No Canadian shortage report is currently matched to this DIN.
Other Canadian products containing OXALIPLATIN
| DIN | Product | Company | Form | Strength | Status |
|---|---|---|---|---|---|
| 02444763 | OXALIPLATIN | PFIZER CANADA ULC | Solution | OXALIPLATIN 5 MG | Marketed |
| 02536757 | OXALIPLATIN INJECTION | EUGIA PHARMA INC. | Solution | OXALIPLATIN 5 MG | Approved |
| 02435071 | OXALIPLATIN INJECTION | TEVA CANADA LIMITED | Solution | OXALIPLATIN 5 MG | Marketed |
| 02436167 | OXALIPLATIN INJECTION | ACCORD HEALTHCARE INC | Solution | OXALIPLATIN 5 MG | Approved |
| 02436957 | OXALIPLATIN INJECTION | SANDOZ CANADA INCORPORATED | Solution | OXALIPLATIN 5 MG | Marketed |
| 02454084 | OXALIPLATIN INJECTION | GENERIC MEDICAL PARTNERS INC | Solution | OXALIPLATIN 5 MG | Approved |
| 02532131 | OXALIPLATIN INJECTION | AURO PHARMA INC | Solution | OXALIPLATIN 5 MG | Approved |
| 02433206 | OXALIPLATIN INJECTION USP | STRIDES PHARMA CANADA INC | Solution | OXALIPLATIN 5 MG | Approved |
| 02457423 | OXALIPLATIN INJECTION, USP | FRESENIUS KABI CANADA LTD | Solution | OXALIPLATIN 5 MG | Marketed |
| 02458403 | OXALIPLATIN INJECTION, USP | DR REDDY'S LABORATORIES LTD | Solution | OXALIPLATIN 5 MG | Marketed |
| 02430533 | ACT OXALIPLATIN | ACTAVIS PHARMA COMPANY | Powder For Solution | OXALIPLATIN 100 MG | Cancelled Pre Market |
| 02432617 | ACT OXALIPLATIN | ACTAVIS PHARMA COMPANY | Solution | OXALIPLATIN 5 MG | Cancelled Post Market |
| 02430525 | ACT OXALIPLATIN | ACTAVIS PHARMA COMPANY | Powder For Solution | OXALIPLATIN 50 MG | Cancelled Pre Market |
| 02296268 | ELOXATIN | SANOFI-AVENTIS CANADA INC | Powder For Solution | OXALIPLATIN 50 MG | Cancelled Post Market |
| 02296276 | ELOXATIN | SANOFI-AVENTIS CANADA INC | Powder For Solution | OXALIPLATIN 100 MG | Cancelled Post Market |
| 02413833 | OXALIPLATIN FOR INJECTION | HOSPIRA HEALTHCARE ULC | Powder For Solution | OXALIPLATIN 50 MG | Cancelled Pre Market |
| 02413841 | OXALIPLATIN FOR INJECTION | HOSPIRA HEALTHCARE ULC | Powder For Solution | OXALIPLATIN 100 MG | Cancelled Pre Market |
| 02431688 | OXALIPLATIN INJECTION | HOSPIRA HEALTHCARE ULC | Solution | OXALIPLATIN 5 MG | Cancelled Pre Market |
| 02437074 | PMS-OXALIPLATIN | PHARMASCIENCE INC | Solution | OXALIPLATIN 5 MG | Cancelled Post Market |
| 02449692 | TARO-OXALIPLATIN | TARO PHARMACEUTICALS INC | Solution | OXALIPLATIN 5 MG | Cancelled Post Market |
| 02446227 | TEVA-OXALIPLATIN INJECTION | TEVA CANADA LIMITED | Solution | OXALIPLATIN 5 MG | Cancelled Pre Market |
Notices of Compliance
| NOC | Date | Submission | Reason |
|---|---|---|---|
| 8845 | 2007-06-15 | New Drug Submission (NDS) |
International API supply for OXALIPLATIN
12 valid EDQM Certificates of Suitability from 12 holders. 17 active FDA Drug Master Files.
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