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=ANDA204253"
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
33342-134-09 33342-134 HUMAN PRESCRIPTION DRUG QUETIAPINE QUETIAPINE TABLET, EXTENDED RELEASE ORAL 20171101 N/A ANDA ANDA204253 Macleods Pharmaceuticals Limited QUETIAPINE FUMARATE 150 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (33342-134-09)
33342-134-15 33342-134 HUMAN PRESCRIPTION DRUG QUETIAPINE QUETIAPINE TABLET, EXTENDED RELEASE ORAL 20171101 N/A ANDA ANDA204253 Macleods Pharmaceuticals Limited QUETIAPINE FUMARATE 150 mg/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (33342-134-15)
33342-136-09 33342-136 HUMAN PRESCRIPTION DRUG QUETIAPINE QUETIAPINE TABLET, EXTENDED RELEASE ORAL 20171101 N/A ANDA ANDA204253 Macleods Pharmaceuticals Limited QUETIAPINE FUMARATE 300 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (33342-136-09)
33342-136-15 33342-136 HUMAN PRESCRIPTION DRUG QUETIAPINE QUETIAPINE TABLET, EXTENDED RELEASE ORAL 20171101 N/A ANDA ANDA204253 Macleods Pharmaceuticals Limited QUETIAPINE FUMARATE 300 mg/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (33342-136-15)
33342-137-09 33342-137 HUMAN PRESCRIPTION DRUG QUETIAPINE QUETIAPINE TABLET, EXTENDED RELEASE ORAL 20171101 N/A ANDA ANDA204253 Macleods Pharmaceuticals Limited QUETIAPINE FUMARATE 400 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (33342-137-09)
33342-137-15 33342-137 HUMAN PRESCRIPTION DRUG QUETIAPINE QUETIAPINE TABLET, EXTENDED RELEASE ORAL 20171101 N/A ANDA ANDA204253 Macleods Pharmaceuticals Limited QUETIAPINE FUMARATE 400 mg/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (33342-137-15)
33342-135-09 33342-135 HUMAN PRESCRIPTION DRUG QUETIAPINE QUETIAPINE TABLET, EXTENDED RELEASE ORAL 20171101 N/A ANDA ANDA204253 Macleods Pharmaceuticals Limited QUETIAPINE FUMARATE 200 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (33342-135-09)
33342-135-15 33342-135 HUMAN PRESCRIPTION DRUG QUETIAPINE QUETIAPINE TABLET, EXTENDED RELEASE ORAL 20171101 N/A ANDA ANDA204253 Macleods Pharmaceuticals Limited QUETIAPINE FUMARATE 200 mg/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (33342-135-15)
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