| Doxorubicin | CA Health Canada | — | Marketed in Canada as DOXORUBICIN HYDROCHLORIDE INJECTION (DIN 02400626) under ATC L01DB01 DOXORUBICIN. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | approved | — | health-canada-dpd |
| Etoposide | CA Health Canada | — | Marketed in Canada as ETOPOSIDE INJECTION (DIN 02552671) under ATC L01CB01 ETOPOSIDE. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | approvedsource: Marketed | Jun 20, 2025 | health-canada-dpd |
| Etoposide | CA Health Canada | — | Marketed in Canada as ETOPOSIDE INJECTION (DIN 02239961) under ATC L01CB01 ETOPOSIDE. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Dormantsince Aug 3, 2017 | Oct 20, 2014 | health-canada-dpd |
| Etoposide | CA Health Canada | — | Marketed in Canada as ETOPOSIDE INJECTION, USP (DIN 02422530) under ATC L01CB01 ETOPOSIDE. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Dormantsince Aug 12, 2020 | Jul 10, 2014 | health-canada-dpd |
| Etoposide | CA Health Canada | — | Marketed in Canada as ETOPOSIDE INJECTION USP (DIN 02380935) under ATC L01CB01 ETOPOSIDE. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Cancelled Post Marketsince Jul 28, 2023 | Sep 4, 2013 | health-canada-dpd |
| Etoposide | CA Health Canada | — | Marketed in Canada as ETOPOSIDE INJECTION, USP (DIN 02241182) under ATC L01CB01 ETOPOSIDE. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Cancelled Post Marketsince Jan 17, 2019 | Dec 28, 1999 | health-canada-dpd |
| Etoposide | CA Health Canada | — | Marketed in Canada as ETOPOSIDE - LIQ IV 20MG/ML (DIN 02227509) under ATC L01CB01 ETOPOSIDE. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Cancelled Post Marketsince Jul 1, 1998 | Jan 28, 1997 | health-canada-dpd |
| Etoposide | CA Health Canada | — | Marketed in Canada as ETOPOSIDE INJECTION (DIN 02080036) under ATC L01CB01 ETOPOSIDE. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | approvedsource: Marketed | Dec 31, 1994 | health-canada-dpd |
| Etoposide | CA Health Canada | — | Marketed in Canada as VEPESID (DIN 00616192) under ATC L01CB01 ETOPOSIDE. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | approvedsource: Marketed | Dec 31, 1984 | health-canada-dpd |
| Etoposide | CA Health Canada | — | Marketed in Canada as VEPESID INJ 20MG/ML (DIN 00523410) under ATC L01CB01 ETOPOSIDE. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Cancelled Post Marketsince Oct 30, 2007 | Dec 31, 1981 | health-canada-dpd |
| Etoposide | CA Health Canada | — | Marketed in Canada as PMS-ETOPOSIDE (DIN 02237871) under ATC L01CB01 ETOPOSIDE. 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 |
| Etoposide | CA Health Canada | — | Marketed in Canada as EPOSIN (DIN 02237428) under ATC L01CB01 ETOPOSIDE. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Cancelled Pre Marketsince Aug 1, 2017 | — | health-canada-dpd |
| Etoposide | CA Health Canada | — | Marketed in Canada as DOM-ETOPOSIDE (DIN 02237872) under ATC L01CB01 ETOPOSIDE. 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 |
| Etoposide | CA Health Canada | — | Marketed in Canada as ETOPOSIDE (DIN 02237873) under ATC L01CB01 ETOPOSIDE. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Cancelled Pre Marketsince Sep 12, 2017 | — | health-canada-dpd |
| Methotrexate | CA Health Canada | — | Marketed in Canada as PMS-METHOTREXATE TABLETS (DIN 02561956) under ATC L01BA01 METHOTREXATE. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | approvedsource: Marketed | Nov 28, 2025 | health-canada-dpd |
| Methotrexate | CA Health Canada | — | Marketed in Canada as JAMP METHOTREXATE TABLETS (DIN 02553740) under ATC L01BA01 METHOTREXATE. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | approvedsource: Marketed | Jun 10, 2025 | health-canada-dpd |
| Methotrexate | CA Health Canada | — | Marketed in Canada as M-METHOTREXATE (DIN 02534916) under ATC L01BA01 METHOTREXATE. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | approvedsource: Marketed | Apr 24, 2024 | health-canada-dpd |
| Methotrexate | CA Health Canada | — | Marketed in Canada as ACH-METHOTREXATE (DIN 02509067) under ATC L01BA01 METHOTREXATE. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | approvedsource: Marketed | Oct 21, 2021 | health-canada-dpd |
| Methotrexate | CA Health Canada | — | Marketed in Canada as METHOTREXATE INJECTION BP (DIN 02464365) under ATC L01BA01 METHOTREXATE. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | approvedsource: Marketed | Oct 22, 2020 | health-canada-dpd |
| Methotrexate | CA Health Canada | — | Marketed in Canada as METHOTREXATE INJECTION BP (DIN 02474735) under ATC L01BA01 METHOTREXATE. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | approvedsource: Marketed | Apr 23, 2019 | health-canada-dpd |
| Methotrexate | CA Health Canada | — | Marketed in Canada as METHOTREXATE INJECTION BP (DIN 02474891) under ATC L01BA01 METHOTREXATE. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | approvedsource: Marketed | Apr 23, 2019 | health-canada-dpd |
| Methotrexate | CA Health Canada | — | Marketed in Canada as METHOTREXATE INJECTION, USP (DIN 02417626) under ATC L01BA01 METHOTREXATE. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Dormantsince Oct 4, 2024 | Aug 14, 2014 | health-canada-dpd |
| Methotrexate | CA Health Canada | — | Marketed in Canada as METHOTREXATE INJECTION, BP (DIN 02422182) under ATC L01BA01 METHOTREXATE. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | approvedsource: Marketed | May 8, 2014 | health-canada-dpd |
| Methotrexate | CA Health Canada | — | Marketed in Canada as METHOTREXATE INJECTION, BP (DIN 02422174) under ATC L01BA01 METHOTREXATE. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | approvedsource: Marketed | May 8, 2014 | health-canada-dpd |
| Methotrexate | CA Health Canada | — | Marketed in Canada as METHOTREXATE INJECTION, BP (DIN 02422190) under ATC L01BA01 METHOTREXATE. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | approvedsource: Marketed | May 8, 2014 | health-canada-dpd |
| Methotrexate | CA Health Canada | — | Marketed in Canada as METHOTREXATE INJECTION, BP (DIN 02422166) under ATC L01BA01 METHOTREXATE. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | approvedsource: Marketed | May 8, 2014 | health-canada-dpd |
| Methotrexate | CA Health Canada | — | Marketed in Canada as METHOTREXATE INJECTION, BP (DIN 02422204) under ATC L01BA01 METHOTREXATE. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | approvedsource: Marketed | May 8, 2014 | health-canada-dpd |
| Methotrexate | CA Health Canada | — | Marketed in Canada as JAMP-METHOTREXATE (DIN 02419173) under ATC L01BA01 METHOTREXATE. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Cancelled Post Marketsince Nov 14, 2022 | Mar 12, 2014 | health-canada-dpd |
| Methotrexate | CA Health Canada | — | Marketed in Canada as METHOTREXATE INJECTION USP (DIN 02398427) under ATC L01BA01 METHOTREXATE. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Cancelled Post Marketsince Jul 28, 2023 | Feb 14, 2013 | health-canada-dpd |
| Methotrexate | CA Health Canada | — | Marketed in Canada as METHOTREXATE INJECTION BP (DIN 02327236) under ATC L01BA01 METHOTREXATE. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | approvedsource: Marketed | Sep 30, 2011 | health-canada-dpd |
| Methotrexate | CA Health Canada | — | Marketed in Canada as METOJECT (DIN 02320053) under ATC L01BA01 METHOTREXATE. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Cancelled Post Marketsince May 19, 2017 | Jan 26, 2009 | health-canada-dpd |
| Methotrexate | CA Health Canada | — | Marketed in Canada as METOJECT (DIN 02320045) under ATC L01BA01 METHOTREXATE. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Cancelled Post Marketsince Jul 17, 2019 | Jan 26, 2009 | health-canada-dpd |
| Methotrexate | CA Health Canada | — | Marketed in Canada as METOJECT (DIN 02320029) under ATC L01BA01 METHOTREXATE. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Cancelled Post Marketsince Jun 29, 2022 | Jan 26, 2009 | health-canada-dpd |
| Methotrexate | CA Health Canada | — | Marketed in Canada as METOJECT (DIN 02320037) under ATC L01BA01 METHOTREXATE. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Cancelled Post Marketsince Apr 23, 2020 | Jan 26, 2009 | health-canada-dpd |
| Methotrexate | CA Health Canada | — | Marketed in Canada as METOJECT (DIN 02304767) under ATC L01BA01 METHOTREXATE. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Cancelled Post Marketsince May 19, 2017 | May 30, 2008 | health-canada-dpd |
| Methotrexate | CA Health Canada | — | Marketed in Canada as METHOTREXATE TABLETS, USP (DIN 02182750) under ATC L01BA01 METHOTREXATE. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | approvedsource: Marketed | Apr 12, 2004 | health-canada-dpd |
| Methotrexate | CA Health Canada | — | Marketed in Canada as RATIO-METHOTREXATE SODIUM (DIN 02244798) under ATC L01BA01 METHOTREXATE. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Cancelled Post Marketsince May 7, 2018 | Nov 14, 2001 | health-canada-dpd |
| Methotrexate | CA Health Canada | — | Marketed in Canada as APO-METHOTREXATE (DIN 02182963) under ATC L01BA01 METHOTREXATE. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | approvedsource: Marketed | Sep 17, 1999 | health-canada-dpd |
| Methotrexate | CA Health Canada | — | Marketed in Canada as METHOTREXATE INJECTION USP (DIN 02182955) under ATC L01BA01 METHOTREXATE. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | approvedsource: Marketed | Jul 13, 1998 | health-canada-dpd |
| Methotrexate | CA Health Canada | — | Marketed in Canada as METHOTREXATE INJECTION USP (DIN 02182777) under ATC L01BA01 METHOTREXATE. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | approvedsource: Marketed | Apr 30, 1998 | health-canada-dpd |
| Methotrexate | CA Health Canada | — | Marketed in Canada as METHOTREXATE INJECTION USP (DIN 02182971) under ATC L01BA01 METHOTREXATE. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | approvedsource: Marketed | Jul 30, 1997 | health-canada-dpd |
| Methotrexate | CA Health Canada | — | Marketed in Canada as METHOTREXATE INJECTION USP (DIN 02182947) under ATC L01BA01 METHOTREXATE. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | approvedsource: Marketed | Jul 30, 1997 | health-canada-dpd |
| Methotrexate | CA Health Canada | — | Marketed in Canada as METHOTREXATE-LIQ IM IV IAR INT IVR 25MG/ML (DIN 02170663) under ATC L01BA01 METHOTREXATE. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Cancelled Post Marketsince Sep 19, 2001 | Feb 4, 1997 | health-canada-dpd |
| Methotrexate | CA Health Canada | — | Marketed in Canada as METHOTREXATE-PWS IM IV IAR INT IVR 20MG/VIAL (DIN 02170655) under ATC L01BA01 METHOTREXATE. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Cancelled Post Marketsince May 22, 2001 | Feb 4, 1997 | health-canada-dpd |
| Methotrexate | CA Health Canada | — | Marketed in Canada as METHOTREXATE (DIN 02170671) under ATC L01BA01 METHOTREXATE. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Cancelled Post Marketsince May 3, 2011 | Jan 24, 1997 | health-canada-dpd |
| Methotrexate | CA Health Canada | — | Marketed in Canada as PMS-METHOTREXATE (DIN 02170698) under ATC L01BA01 METHOTREXATE. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | approvedsource: Marketed | Nov 15, 1996 | health-canada-dpd |
| Methotrexate | CA Health Canada | — | Marketed in Canada as METHOTREXATE SODIUM INJECTION USP (DIN 02161168) under ATC L01BA01 METHOTREXATE. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Cancelled Post Marketsince Aug 2, 2006 | Sep 5, 1996 | health-canada-dpd |
| Methotrexate | CA Health Canada | — | Marketed in Canada as METHOTREXATE SODIUM INJECTION (DIN 02099705) under ATC L01BA01 METHOTREXATE. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | approvedsource: Marketed | Dec 31, 1995 | health-canada-dpd |
| Methotrexate | CA Health Canada | — | Marketed in Canada as METHOTREXATE SODIUM INJ 25MG/ML USP (DIN 01911457) under ATC L01BA01 METHOTREXATE. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Cancelled Post Marketsince Aug 10, 1999 | Dec 31, 1992 | health-canada-dpd |
| Methotrexate | CA Health Canada | — | Marketed in Canada as METHOTREXATE TAB 2.5MG USP (DIN 00632619) under ATC L01BA01 METHOTREXATE. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Cancelled Post Marketsince Aug 1, 2000 | Dec 31, 1991 | health-canada-dpd |