| Cisplatin | CA Health Canada | — | Marketed in Canada as CISPLATIN INJECTION, MYLAN STD. (DIN 02396890) under ATC L01XA01 CISPLATIN. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Cancelled Post Marketsince Jul 6, 2016 | Jun 12, 2013 | health-canada-dpd |
| Cisplatin | CA Health Canada | — | Marketed in Canada as CISPLATIN INJECTION, BP (DIN 02355183) under ATC L01XA01 CISPLATIN. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | approvedsource: Marketed | Apr 10, 2012 | health-canada-dpd |
| Cisplatin | CA Health Canada | — | Marketed in Canada as CISPLATIN INJECTION BP (DIN 02366711) under ATC L01XA01 CISPLATIN. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Cancelled Post Marketsince Jul 25, 2022 | Sep 29, 2011 | health-canada-dpd |
| Cisplatin | CA Health Canada | — | Marketed in Canada as CISPLATIN INJECTION BP (DIN 02126613) under ATC L01XA01 CISPLATIN. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | approvedsource: Marketed | May 9, 1997 | health-canada-dpd |
| Cisplatin | CA Health Canada | — | Marketed in Canada as PLATINOL AQ INJ 1MG/ML (DIN 00788740) under ATC L01XA01 CISPLATIN. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Cancelled Post Marketsince Jul 30, 2001 | Dec 31, 1988 | health-canada-dpd |
| Cisplatin | CA Health Canada | — | Marketed in Canada as CISPLATIN INJ 1MG/ML (DIN 00692743) under ATC L01XA01 CISPLATIN. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Cancelled Post Marketsince Aug 13, 1998 | Dec 31, 1986 | health-canada-dpd |
| Cisplatin | CA Health Canada | — | Marketed in Canada as CISPLATIN INJ 0.5MG/ML (DIN 00644293) under ATC L01XA01 CISPLATIN. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Cancelled Post Marketsince Sep 10, 1996 | Dec 31, 1985 | health-canada-dpd |
| Cisplatin | CA Health Canada | — | Marketed in Canada as CISPLATIN INJECTION (DIN 02393832) under ATC L01XA01 CISPLATIN. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | approved | — | health-canada-dpd |
| Cisplatin | CA Health Canada | — | Marketed in Canada as CISPLATIN INJECTION (DIN 02422034) under ATC L01XA01 CISPLATIN. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | approved | — | health-canada-dpd |
| Cisplatin | CA Health Canada | — | Marketed in Canada as PMS-CISPLATIN (DIN 02409194) under ATC L01XA01 CISPLATIN. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Cancelled Pre Marketsince Aug 3, 2017 | — | health-canada-dpd |
| Cisplatin | CA Health Canada | — | Marketed in Canada as CISPLATIN INJECTION (DIN 02409186) under ATC L01XA01 CISPLATIN. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | approved | — | health-canada-dpd |
| Docetaxel | CA Health Canada | — | Marketed in Canada as DOCETAXEL INJECTION (DIN 02458020) under ATC L01CD02 DOCETAXEL. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | approvedsource: Marketed | Oct 17, 2017 | health-canada-dpd |
| Docetaxel | CA Health Canada | — | Marketed in Canada as DOCETAXEL INJECTION (DIN 02439336) under ATC L01CD02 DOCETAXEL. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | approvedsource: Marketed | Jun 2, 2016 | health-canada-dpd |
| Docetaxel | CA Health Canada | — | Marketed in Canada as DOCETAXEL INJECTION (DIN 02437031) under ATC L01CD02 DOCETAXEL. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Dormantsince Oct 29, 2025 | Feb 27, 2015 | health-canada-dpd |
| Docetaxel | CA Health Canada | — | Marketed in Canada as DOCETAXEL INJECTION (DIN 02412225) under ATC L01CD02 DOCETAXEL. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Cancelled Post Marketsince May 17, 2018 | Mar 28, 2014 | health-canada-dpd |
| Docetaxel | CA Health Canada | — | Marketed in Canada as DOCETAXEL INJECTION (DIN 02412233) under ATC L01CD02 DOCETAXEL. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Cancelled Post Marketsince May 17, 2018 | Mar 28, 2014 | health-canada-dpd |
| Docetaxel | CA Health Canada | — | Marketed in Canada as DOCETAXEL INJECTION USP (DIN 02361957) under ATC L01CD02 DOCETAXEL. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | approvedsource: Marketed | Mar 1, 2011 | health-canada-dpd |
| Docetaxel | CA Health Canada | — | Marketed in Canada as TAXOTERE (DIN 02177099) under ATC L01CD02 DOCETAXEL. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Cancelled Post Marketsince Apr 30, 2018 | Dec 31, 1995 | health-canada-dpd |
| Docetaxel | CA Health Canada | — | Marketed in Canada as TAXOTERE (DIN 02177080) under ATC L01CD02 DOCETAXEL. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Cancelled Post Marketsince Jul 31, 2020 | Dec 31, 1995 | health-canada-dpd |
| Docetaxel | CA Health Canada | — | Marketed in Canada as TARO-DOCETAXEL (DIN 02465647) under ATC L01CD02 DOCETAXEL. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Cancelled Pre Marketsince Jul 11, 2022 | — | health-canada-dpd |
| Docetaxel | CA Health Canada | — | Marketed in Canada as ACT DOCETAXEL 40 MG/ML (DIN 02441845) under ATC L01CD02 DOCETAXEL. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Cancelled Pre Marketsince Jul 24, 2020 | — | health-canada-dpd |
| Docetaxel | CA Health Canada | — | Marketed in Canada as ACT DOCETAXEL 40 MG/ML (DIN 02444410) under ATC L01CD02 DOCETAXEL. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Cancelled Pre Marketsince Jul 24, 2020 | — | health-canada-dpd |
| Docetaxel | CA Health Canada | — | Marketed in Canada as TARO-DOCETAXEL (DIN 02465655) under ATC L01CD02 DOCETAXEL. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Cancelled Pre Marketsince Jul 11, 2022 | — | health-canada-dpd |
| Docetaxel | CA Health Canada | — | Marketed in Canada as PMS-DOCETAXEL (DIN 02436361) under ATC L01CD02 DOCETAXEL. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Cancelled Pre Marketsince Mar 15, 2023 | — | health-canada-dpd |
| Docetaxel | CA Health Canada | — | Marketed in Canada as PMS-DOCETAXEL (DIN 02436388) under ATC L01CD02 DOCETAXEL. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Cancelled Pre Marketsince Mar 15, 2023 | — | health-canada-dpd |
| Docetaxel | CA Health Canada | — | Marketed in Canada as TARO-DOCETAXEL (DIN 02465531) under ATC L01CD02 DOCETAXEL. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Cancelled Pre Marketsince Jul 11, 2022 | — | health-canada-dpd |
| Doxorubicin | CA Health Canada | — | Marketed in Canada as TARO-DOXORUBICIN LIPOSOMAL (DIN 02493020) under ATC L01DB01 DOXORUBICIN. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | approvedsource: Marketed | May 19, 2020 | health-canada-dpd |
| Doxorubicin | CA Health Canada | — | Marketed in Canada as DOXORUBICIN HYDROCHLORIDE INJECTION (DIN 02375710) under ATC L01DB01 DOXORUBICIN. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Cancelled Post Marketsince Apr 21, 2021 | Apr 10, 2015 | health-canada-dpd |
| Doxorubicin | CA Health Canada | — | Marketed in Canada as DOXORUBICIN HYDROCHLORIDE INJECTION, USP (DIN 02413973) under ATC L01DB01 DOXORUBICIN. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Dormantsince Jun 1, 2021 | Jan 8, 2015 | health-canada-dpd |
| Doxorubicin | CA Health Canada | — | Marketed in Canada as DOXORUBICIN INJECTION, BP (DIN 02381982) under ATC L01DB01 DOXORUBICIN. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | approvedsource: Marketed | Dec 16, 2014 | health-canada-dpd |
| Doxorubicin | CA Health Canada | — | Marketed in Canada as DOXORUBICIN (DIN 02410397) under ATC L01DB01 DOXORUBICIN. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | approvedsource: Marketed | May 21, 2014 | health-canada-dpd |
| Doxorubicin | CA Health Canada | — | Marketed in Canada as DOXORUBICIN HYDROCHLORIDE INJECTION (DIN 02409275) under ATC L01DB01 DOXORUBICIN. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | approvedsource: Marketed | Feb 27, 2014 | health-canada-dpd |
| Doxorubicin | CA Health Canada | — | Marketed in Canada as MYOCET (DIN 02245015) under ATC L01DB01 DOXORUBICIN. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Dormantsince Sep 7, 2018 | Dec 21, 2001 | health-canada-dpd |
| Doxorubicin | CA Health Canada | — | Marketed in Canada as CAELYX (DIN 02238389) under ATC L01DB01 DOXORUBICIN. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | approvedsource: Marketed | Aug 19, 1998 | health-canada-dpd |
| Doxorubicin | CA Health Canada | — | Marketed in Canada as DOXORUBICIN HYDROCHLORIDE FOR INJECTION USP (DIN 02194457) under ATC L01DB01 DOXORUBICIN. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Cancelled Pre Marketsince May 9, 2024 | Mar 12, 1998 | health-canada-dpd |
| Doxorubicin | CA Health Canada | — | Marketed in Canada as DOXORUBICIN HYDROCHLORIDE INJECTION (DIN 02230108) under ATC L01DB01 DOXORUBICIN. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Cancelled Post Marketsince May 2, 2018 | Sep 12, 1997 | health-canada-dpd |
| Doxorubicin | CA Health Canada | — | Marketed in Canada as DOXORUBICIN HYDROCHLORIDE FOR INJECTION USP (DIN 02194465) under ATC L01DB01 DOXORUBICIN. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | approvedsource: Marketed | Jul 30, 1997 | health-canada-dpd |
| Doxorubicin | CA Health Canada | — | Marketed in Canada as DOXORUBICIN HYDROCHLORIDE FOR INJECTION USP (DIN 02194473) under ATC L01DB01 DOXORUBICIN. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | approvedsource: Marketed | May 8, 1997 | health-canada-dpd |
| Doxorubicin | CA Health Canada | — | Marketed in Canada as ADRIAMYCIN RDF (DIN 02065657) under ATC L01DB01 DOXORUBICIN. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Cancelled Post Marketsince Aug 2, 2006 | Dec 31, 1996 | health-canada-dpd |
| Doxorubicin | CA Health Canada | — | Marketed in Canada as ADRIAMYCIN RDF (DIN 02069563) under ATC L01DB01 DOXORUBICIN. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Cancelled Post Marketsince Aug 2, 2006 | Dec 31, 1996 | health-canada-dpd |
| Doxorubicin | CA Health Canada | — | Marketed in Canada as DOXORUBICIN HCL FOR INJ. U.S.P. 150MG/VIAL (DIN 02093081) under ATC L01DB01 DOXORUBICIN. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Cancelled Post Marketsince Aug 14, 1997 | Dec 31, 1995 | health-canada-dpd |
| Doxorubicin | CA Health Canada | — | Marketed in Canada as DOXORUBICIN HCL FOR INJ. U.S.P. 50MG/VIAL (DIN 02093073) under ATC L01DB01 DOXORUBICIN. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Cancelled Post Marketsince Aug 14, 1997 | Dec 31, 1995 | health-canada-dpd |
| Doxorubicin | CA Health Canada | — | Marketed in Canada as DOXORUBICIN HCL FOR INJ. U.S.P. 10MG/VIAL (DIN 02093057) under ATC L01DB01 DOXORUBICIN. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Cancelled Post Marketsince Aug 13, 1998 | Dec 31, 1995 | health-canada-dpd |
| Doxorubicin | CA Health Canada | — | Marketed in Canada as ADRIAMYCIN RDF (DIN 02069555) under ATC L01DB01 DOXORUBICIN. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Cancelled Post Marketsince Aug 2, 2006 | Dec 31, 1995 | health-canada-dpd |
| Doxorubicin | CA Health Canada | — | Marketed in Canada as ADRIAMYCIN PFS (DIN 02071002) under ATC L01DB01 DOXORUBICIN. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Dormantsince Aug 2, 2017 | Dec 31, 1995 | health-canada-dpd |
| Doxorubicin | CA Health Canada | — | Marketed in Canada as ADRIAMYCIN RDF INJ 150MG/VIAL (DIN 00768766) under ATC L01DB01 DOXORUBICIN. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Cancelled Post Marketsince Sep 10, 1996 | Dec 31, 1988 | health-canada-dpd |
| Doxorubicin | CA Health Canada | — | Marketed in Canada as ADRIAMYCIN RDF INJ 10MG/VIAL (DIN 00357391) under ATC L01DB01 DOXORUBICIN. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Cancelled Post Marketsince Sep 10, 1996 | Dec 31, 1976 | health-canada-dpd |
| Doxorubicin | CA Health Canada | — | Marketed in Canada as ADRIAMYCIN RDF INJ 50MG/VIAL (DIN 00353078) under ATC L01DB01 DOXORUBICIN. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Cancelled Post Marketsince Sep 10, 1996 | Dec 31, 1976 | health-canada-dpd |
| Doxorubicin | CA Health Canada | — | Marketed in Canada as DOXORUBICIN HYDROCHLORIDE FOR INJECTION USP (DIN 02467240) under ATC L01DB01 DOXORUBICIN. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Cancelled Pre Marketsince Jul 14, 2026 | — | health-canada-dpd |
| Doxorubicin | CA Health Canada | — | Marketed in Canada as PEGYLATED LIPOSOMAL DOXORUBICIN HYDROCHLORIDE FOR INJECTION (DIN 02544857) under ATC L01DB01 DOXORUBICIN. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | approved | — | health-canada-dpd |