美国药品NDC(国家药品编码)与药品说明书数据库(U.S. FDA National Drug Code DataBase)
检索条件:" 注册申请号=ANDA202376"
NDC包装代码 产品NDC 产品类型 商品名 通用名 剂型 给药途径 上市日期 结束日期 市场类别 申请号 标签持有者 活性成分 规格 包装描述
63187-555-30 63187-555 HUMAN PRESCRIPTION DRUG Rabeprazole sodium Rabeprazole sodium TABLET, DELAYED RELEASE ORAL 20181201 N/A ANDA ANDA202376 Proficient Rx LP RABEPRAZOLE SODIUM 20 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-555-30)
63187-555-60 63187-555 HUMAN PRESCRIPTION DRUG Rabeprazole sodium Rabeprazole sodium TABLET, DELAYED RELEASE ORAL 20181201 N/A ANDA ANDA202376 Proficient Rx LP RABEPRAZOLE SODIUM 20 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-555-60)
63187-555-90 63187-555 HUMAN PRESCRIPTION DRUG Rabeprazole sodium Rabeprazole sodium TABLET, DELAYED RELEASE ORAL 20181201 N/A ANDA ANDA202376 Proficient Rx LP RABEPRAZOLE SODIUM 20 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-555-90)
61919-225-60 61919-225 HUMAN PRESCRIPTION DRUG RABERPRAZOLE SODIUM D/R RABERPRAZOLE SODIUM D/R TABLET, DELAYED RELEASE ORAL 20190807 N/A ANDA ANDA202376 Direct_Rx RABEPRAZOLE SODIUM 20 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (61919-225-60)
61919-225-90 61919-225 HUMAN PRESCRIPTION DRUG RABERPRAZOLE SODIUM D/R RABERPRAZOLE SODIUM D/R TABLET, DELAYED RELEASE ORAL 20190807 N/A ANDA ANDA202376 Direct_Rx RABEPRAZOLE SODIUM 20 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (61919-225-90)
13668-107-30 13668-107 HUMAN PRESCRIPTION DRUG Rabeprazole sodium Rabeprazole sodium TABLET, DELAYED RELEASE ORAL 20131108 N/A ANDA ANDA202376 Torrent Pharmaceuticals Limited RABEPRAZOLE SODIUM 20 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (13668-107-30)
13668-107-90 13668-107 HUMAN PRESCRIPTION DRUG Rabeprazole sodium Rabeprazole sodium TABLET, DELAYED RELEASE ORAL 20131108 N/A ANDA ANDA202376 Torrent Pharmaceuticals Limited RABEPRAZOLE SODIUM 20 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (13668-107-90)
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