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=NDA022421"
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
0597-0109-30 0597-0109 HUMAN PRESCRIPTION DRUG Mirapex ER pramipexole dihydrochloride TABLET, EXTENDED RELEASE ORAL 20100222 20240731 NDA NDA022421 Boehringer Ingelheim Pharmaceuticals, Inc. PRAMIPEXOLE DIHYDROCHLORIDE .375 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (0597-0109-30) / 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC
0597-0115-30 0597-0115 HUMAN PRESCRIPTION DRUG Mirapex ER pramipexole dihydrochloride TABLET, EXTENDED RELEASE ORAL 20100222 20240831 NDA NDA022421 Boehringer Ingelheim Pharmaceuticals, Inc. PRAMIPEXOLE DIHYDROCHLORIDE 3 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (0597-0115-30) / 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC
0597-0116-30 0597-0116 HUMAN PRESCRIPTION DRUG Mirapex ER pramipexole dihydrochloride TABLET, EXTENDED RELEASE ORAL 20100222 20240630 NDA NDA022421 Boehringer Ingelheim Pharmaceuticals, Inc. PRAMIPEXOLE DIHYDROCHLORIDE 4.5 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (0597-0116-30) / 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC
0597-0285-30 0597-0285 HUMAN PRESCRIPTION DRUG Mirapex ER pramipexole dihydrochloride TABLET, EXTENDED RELEASE ORAL 20100222 20240731 NDA NDA022421 Boehringer Ingelheim Pharmaceuticals, Inc. PRAMIPEXOLE DIHYDROCHLORIDE .75 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (0597-0285-30) / 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC
0597-0286-30 0597-0286 HUMAN PRESCRIPTION DRUG Mirapex ER pramipexole dihydrochloride TABLET, EXTENDED RELEASE ORAL 20110618 20240831 NDA NDA022421 Boehringer Ingelheim Pharmaceuticals, Inc. PRAMIPEXOLE DIHYDROCHLORIDE 2.25 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (0597-0286-30) / 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC
0597-0287-30 0597-0287 HUMAN PRESCRIPTION DRUG Mirapex ER pramipexole dihydrochloride TABLET, EXTENDED RELEASE ORAL 20110618 20240831 NDA NDA022421 Boehringer Ingelheim Pharmaceuticals, Inc. PRAMIPEXOLE DIHYDROCHLORIDE 3.75 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (0597-0287-30) / 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase