美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=OXALIPLATIN"
商品名 申请号 产品号 申请类型 活性成分 剂型/给药途径 规格/剂量 RLD RS 申请号原始批准/暂定批准日期 产品号批准日期 申请人 市场状态
OXALIPLATIN 091358 003 ANDA OXALIPLATIN INJECTABLE;INTRAVENOUS 200MG/40ML (5MG/ML) No No 2017/11/14 2017/11/14 MYLAN LABS LTD Discontinued
OXALIPLATIN 204880 001 ANDA OXALIPLATIN INJECTABLE;INTRAVENOUS 50MG/10ML (5MG/ML) No No 2018/03/05 2018/03/05 ACTAVIS Prescription
OXALIPLATIN 204880 002 ANDA OXALIPLATIN INJECTABLE;INTRAVENOUS 100MG/20ML (5MG/ML) No No 2018/03/05 2018/03/05 ACTAVIS Prescription
OXALIPLATIN 207562 001 ANDA OXALIPLATIN INJECTABLE;INTRAVENOUS 50MG/10ML (5MG/ML) No No 2018/10/16 2018/10/16 NOVAST LABS Prescription
OXALIPLATIN 207562 002 ANDA OXALIPLATIN INJECTABLE;INTRAVENOUS 100MG/20ML (5MG/ML) No No 2018/10/16 2018/10/16 NOVAST LABS Prescription
OXALIPLATIN 202922 001 ANDA OXALIPLATIN INJECTABLE;INTRAVENOUS 50MG/10ML (5MG/ML) No No 2019/02/15 2014/04/08 SUN PHARM Discontinued
OXALIPLATIN 202922 002 ANDA OXALIPLATIN INJECTABLE;INTRAVENOUS 100MG/20ML (5MG/ML) No No 2019/02/15 2014/04/08 SUN PHARM Discontinued
OXALIPLATIN 202922 003 ANDA OXALIPLATIN INJECTABLE;INTRAVENOUS 200MG/40ML (5MG/ML) No No 2019/02/15 2019/02/15 SUN PHARM Discontinued
OXALIPLATIN 217348 001 ANDA OXALIPLATIN INJECTABLE;INTRAVENOUS 50MG/10ML (5MG/ML) No No 2024/01/11 2024/01/11 MEITHEAL Prescription
OXALIPLATIN 217348 002 ANDA OXALIPLATIN INJECTABLE;INTRAVENOUS 100MG/20ML (5MG/ML) No No 2024/01/11 2024/01/11 MEITHEAL Prescription
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