美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=RANITIDINE"
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
RANITIDINE HYDROCHLORIDE 210681 002 ANDA RANITIDINE HYDROCHLORIDE CAPSULE;ORAL EQ 300MG BASE No No 2018/11/23 2018/11/23 NOVITIUM PHARMA Prescription
RANITIDINE HYDROCHLORIDE 211289 001 ANDA RANITIDINE HYDROCHLORIDE TABLET;ORAL EQ 150MG BASE No No 2019/01/31 2019/01/31 VKT PHARMA Prescription
RANITIDINE HYDROCHLORIDE 211289 002 ANDA RANITIDINE HYDROCHLORIDE TABLET;ORAL EQ 300MG BASE No No 2019/01/31 2019/01/31 VKT PHARMA Prescription
RANITIDINE HYDROCHLORIDE 211893 001 ANDA RANITIDINE HYDROCHLORIDE CAPSULE;ORAL EQ 150MG BASE No No 2019/04/05 2019/04/05 APPCO Discontinued
RANITIDINE HYDROCHLORIDE 211893 002 ANDA RANITIDINE HYDROCHLORIDE CAPSULE;ORAL EQ 300MG BASE No No 2019/04/05 2019/04/05 APPCO Discontinued
RANITIDINE HYDROCHLORIDE 210228 001 ANDA RANITIDINE HYDROCHLORIDE TABLET;ORAL EQ 150MG BASE No No 2019/08/30 2019/08/30 UNIQUE PHARM LABS Over-the-counter
RANITIDINE HYDROCHLORIDE 210250 001 ANDA RANITIDINE HYDROCHLORIDE TABLET;ORAL EQ 75MG BASE No No 2019/08/30 2019/08/30 UNIQUE PHARM LABS Over-the-counter
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