| Olaparib | US FDA | — | Efficacy supplement 2020-12-07 (see label) | approved | Dec 7, 2020 | openfda |
| Olaparib | US FDA | — | Efficacy supplement 2020-05-19 (see label) | approved | May 19, 2020 | openfda |
| Olaparib | US FDA | — | Efficacy supplement 2020-05-08 (see label) | approved | May 8, 2020 | openfda |
| Olaparib | US FDA | — | Efficacy supplement 2019-12-27 (see label) | approved | Dec 27, 2019 | openfda |
| Olaparib | US FDA | — | Efficacy supplement 2019-07-01 (see label) | approved | Jul 1, 2019 | openfda |
| Olaparib | US FDA | — | Efficacy supplement 2018-12-19 (see label) | approved | Dec 19, 2018 | openfda |
| Olaparib | US FDA | — | Efficacy supplement 2018-09-26 (see label) | approved | Sep 26, 2018 | openfda |
| Olaparib | US FDA | — | Efficacy supplement 2018-01-12 (see label) | approved | Jan 12, 2018 | openfda |
| Olaparib | US FDA | Pancreatic Adenocarcinoma | Pancreatic cancer • for the maintenance treatment of adult patients with deleterious or suspected deleterious gBRCA m metastatic pancreatic adenocarcinoma whose disease has not progressed on at least 16 weeks of a first-line platinum-based chemotherapy regimen. Select patients for therapy based on an FDA-approved companion diagnostic for Lynparza. | approved | Aug 17, 2017 | openfda |
| Olaparib | US FDA | — | Ovarian cancer • for the maintenance treatment of adult patients with deleterious or suspected deleterious germline or somatic BRCA -mutated advanced epithelial ovarian, fallopian tube or primary peritoneal cancer who are in complete or partial response to first-line platinum-based chemotherapy. Select patients for therapy based on an FDA-approved companion diagnostic for Lynparza. | approved | Aug 17, 2017 | openfda |
| Olaparib | US FDA | Castration-Resistant Prostate Carcinoma | in combination with abiraterone and prednisone or prednisolone for the treatment of adult patients with deleterious or suspected deleterious BRCA -mutated ( BRCA m) metastatic castration-resistant prostate cancer (mCRPC). Select patients for therapy based on an FDA-approved companion diagnostic for Lynparza. | approved | Aug 17, 2017 | openfda |
| Olaparib | US FDA | Malignant Breast Neoplasm | Breast cancer • for the adjuvant treatment of adult patients with deleterious or suspected deleterious g BRCA m human epidermal growth factor receptor 2 (HER2)-negative high risk early breast cancer who have been treated with neoadjuvant or adjuvant chemotherapy. Select patients for therapy based on an FDA-approved companion diagnostic for Lynparza. | approved | Aug 17, 2017 | openfda |
| Olaparib | US FDA | Castration-Resistant Prostate Carcinoma | Prostate cancer • for the treatment of adult patients with deleterious or suspected deleterious germline or somatic homologous recombination repair (HRR) gene-mutated metastatic castration-resistant prostate cancer (mCRPC) who have progressed following prior treatment with enzalutamide or abiraterone. Select patients for therapy based on an FDA-approved companion diagnostic for Lynparza. | approved | Aug 17, 2017 | openfda |
| Olaparib | US FDA | Malignant Peritoneal Neoplasm | in combination with bevacizumab for the maintenance treatment of adult patients with advanced epithelial ovarian, fallopian tube or primary peritoneal cancer who are in complete or partial response to first-line platinum-based chemotherapy and whose cancer is associated with homologous recombination deficiency (HRD)-positive status defined by either: • a deleterious or suspected deleterious BRCA mutation, and/or • genomic instability. Select patients for therapy based on an FDA-approved companion diagnostic for Lynparza. | approved | Aug 17, 2017 | openfda |
| Olaparib | US FDA | Malignant Peritoneal Neoplasm | for the maintenance treatment of adult patients with deleterious or suspected deleterious germline or somatic BRCA-mutated recurrent epithelial ovarian, fallopian tube or primary peritoneal cancer, who are in complete or partial response to platinum-based chemotherapy. Select patients for therapy based on an FDA-approved companion diagnostic for Lynparza. | approved | Aug 17, 2017 | openfda |
| Olaparib | US FDA | Hormone Receptor-Positive Breast Carcinoma | for the treatment of adult patients with deleterious or suspected deleterious gBRCA m, HER2-negative metastatic breast cancer who have been treated with chemotherapy in the neoadjuvant, adjuvant or metastatic setting. Patients with hormone receptor (HR)-positive breast cancer should have been treated with a prior endocrine therapy or be considered inappropriate for endocrine therapy. Select patients for therapy based on an FDA-approved companion diagnostic for Lynparza. | approved | Aug 17, 2017 | openfda |
| Oxaliplatin | CA Health Canada | — | Marketed in Canada as OXALIPLATIN INJECTION, USP (DIN 02458403) under ATC L01XA03 OXALIPLATIN. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | approvedsource: Marketed | Jul 13, 2022 | health-canada-dpd |
| Oxaliplatin | CA Health Canada | — | Marketed in Canada as OXALIPLATIN INJECTION, USP (DIN 02457423) under ATC L01XA03 OXALIPLATIN. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | approvedsource: Marketed | Mar 31, 2022 | health-canada-dpd |
| Oxaliplatin | CA Health Canada | — | Marketed in Canada as TARO-OXALIPLATIN (DIN 02449692) under ATC L01XA03 OXALIPLATIN. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Cancelled Post Marketsince Sep 18, 2024 | Feb 15, 2017 | health-canada-dpd |
| Oxaliplatin | CA Health Canada | — | Marketed in Canada as OXALIPLATIN INJECTION (DIN 02436167) under ATC L01XA03 OXALIPLATIN. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | approved | Jan 2, 2016 | health-canada-dpd |
| Oxaliplatin | CA Health Canada | — | Marketed in Canada as OXALIPLATIN INJECTION (DIN 02436957) under ATC L01XA03 OXALIPLATIN. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | approvedsource: Marketed | Dec 17, 2015 | health-canada-dpd |
| Oxaliplatin | CA Health Canada | — | Marketed in Canada as OXALIPLATIN (DIN 02444763) under ATC L01XA03 OXALIPLATIN. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | approvedsource: Marketed | Dec 17, 2015 | health-canada-dpd |
| Oxaliplatin | CA Health Canada | — | Marketed in Canada as PMS-OXALIPLATIN (DIN 02437074) under ATC L01XA03 OXALIPLATIN. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Cancelled Post Marketsince Jul 4, 2025 | Dec 16, 2015 | health-canada-dpd |
| Oxaliplatin | CA Health Canada | — | Marketed in Canada as OXALIPLATIN INJECTION (DIN 02435071) under ATC L01XA03 OXALIPLATIN. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | approvedsource: Marketed | Dec 16, 2015 | health-canada-dpd |
| Oxaliplatin | CA Health Canada | — | Marketed in Canada as ACT OXALIPLATIN (DIN 02432617) under ATC L01XA03 OXALIPLATIN. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Cancelled Post Marketsince Jul 9, 2018 | Dec 16, 2015 | health-canada-dpd |
| Oxaliplatin | CA Health Canada | — | Marketed in Canada as ELOXATIN (DIN 02296268) under ATC L01XA03 OXALIPLATIN. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Cancelled Post Marketsince Aug 3, 2016 | Jun 27, 2008 | health-canada-dpd |
| Oxaliplatin | CA Health Canada | — | Marketed in Canada as ELOXATIN (DIN 02296276) under ATC L01XA03 OXALIPLATIN. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Cancelled Post Marketsince Aug 4, 2016 | Jun 27, 2008 | health-canada-dpd |
| Oxaliplatin | CA Health Canada | — | Marketed in Canada as ELOXATIN (DIN 02296284) under ATC L01XA03 OXALIPLATIN. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Cancelled Post Marketsince Nov 9, 2018 | Jul 17, 2007 | health-canada-dpd |
| Oxaliplatin | CA Health Canada | — | Marketed in Canada as OXALIPLATIN INJECTION (DIN 02536757) under ATC L01XA03 OXALIPLATIN. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | approved | — | health-canada-dpd |
| Oxaliplatin | CA Health Canada | — | Marketed in Canada as OXALIPLATIN INJECTION (DIN 02431688) under ATC L01XA03 OXALIPLATIN. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Cancelled Pre Marketsince Oct 26, 2018 | — | health-canada-dpd |
| Oxaliplatin | CA Health Canada | — | Marketed in Canada as ACT OXALIPLATIN (DIN 02430533) under ATC L01XA03 OXALIPLATIN. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Cancelled Pre Marketsince Jul 24, 2018 | — | health-canada-dpd |
| Oxaliplatin | CA Health Canada | — | Marketed in Canada as ACT OXALIPLATIN (DIN 02430525) under ATC L01XA03 OXALIPLATIN. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Cancelled Pre Marketsince Jul 24, 2018 | — | health-canada-dpd |
| Oxaliplatin | CA Health Canada | — | Marketed in Canada as TEVA-OXALIPLATIN INJECTION (DIN 02446227) under ATC L01XA03 OXALIPLATIN. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Cancelled Pre Marketsince Jul 29, 2021 | — | health-canada-dpd |
| Oxaliplatin | CA Health Canada | — | Marketed in Canada as OXALIPLATIN FOR INJECTION (DIN 02413833) under ATC L01XA03 OXALIPLATIN. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Cancelled Pre Marketsince Oct 25, 2018 | — | health-canada-dpd |
| Oxaliplatin | CA Health Canada | — | Marketed in Canada as OXALIPLATIN INJECTION USP (DIN 02433206) under ATC L01XA03 OXALIPLATIN. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | approved | — | health-canada-dpd |
| Oxaliplatin | CA Health Canada | — | Marketed in Canada as OXALIPLATIN INJECTION (DIN 02454084) under ATC L01XA03 OXALIPLATIN. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | approved | — | health-canada-dpd |
| Oxaliplatin | CA Health Canada | — | Marketed in Canada as OXALIPLATIN INJECTION (DIN 02532131) under ATC L01XA03 OXALIPLATIN. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | approved | — | health-canada-dpd |
| Oxaliplatin | CA Health Canada | — | Marketed in Canada as OXALIPLATIN FOR INJECTION (DIN 02413841) under ATC L01XA03 OXALIPLATIN. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Cancelled Pre Marketsince Oct 25, 2018 | — | health-canada-dpd |
| Oxaliplatin | US FDA | Malignant Colon Neoplasm | adjuvant treatment of stage III colon cancer in patients who have undergone complete resection of the primary tumor. | approved | Aug 7, 2009 | openfda |
| Oxaliplatin | US FDA | Malignant Colorectal Neoplasm | treatment of advanced colorectal cancer. Oxaliplatin is a platinum-based drug used in combination with infusional fluorouracil and leucovorin, which is indicated for: | approved | Aug 7, 2009 | openfda |
| Oxaliplatin | US FDA | Malignant Colon Neoplasm | adjuvant treatment of stage III colon cancer in patients who have undergone complete resection of the primary tumor. ( 1 ) | approved | Aug 7, 2009 | openfda |
| Oxaliplatin | US FDA | Malignant Colorectal Neoplasm | treatment of advanced colorectal cancer. ( 1 ) | approved | Aug 7, 2009 | openfda |
| Rucaparib | EU EMA | Malignant Peritoneal Neoplasm | Rubraca is indicated as monotherapy for the maintenance treatment of adult patients with advanced (FIGO Stages III and IV) high-grade epithelial ovarian, fallopian tube, or primary peritoneal cancer who are in response (complete or partial) following completion of first-line platinum-based chemotherapy. Rubraca is indicated as monotherapy for the maintenance treatment of adult patients with platinum-sensitive relapsed high-grade epithelial ovarian, fallopian tube, or primary peritoneal cancer who are in response (complete or partial) to platinum-based chemotherapy. | approved | May 23, 2018 | ema |
| Rucaparib | US FDA | — | Efficacy supplement 2025-12-17 (see label) | approved | Dec 17, 2025 | openfda |
| Rucaparib | US FDA | — | Efficacy supplement 2025-12-17 (see label) | approved | Dec 17, 2025 | openfda |
| Rucaparib | US FDA | — | Efficacy supplement 2022-12-21 (see label) | approved | Dec 21, 2022 | openfda |
| Rucaparib | US FDA | — | Efficacy supplement 2022-06-10 (see label) | approved | Jun 10, 2022 | openfda |
| Rucaparib | US FDA | — | Efficacy supplement 2020-10-08 (see label) | approved | Oct 8, 2020 | openfda |
| Rucaparib | US FDA | — | Efficacy supplement 2020-05-15 (see label) | approved | May 15, 2020 | openfda |
| Rucaparib | US FDA | — | Efficacy supplement 2018-04-06 (see label) | approved | Apr 6, 2018 | openfda |