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=NDA021925"
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
64764-302-30 64764-302 HUMAN PRESCRIPTION DRUG Duetact pioglitazone and glimepiride TABLET ORAL 20060728 N/A NDA NDA021925 Takeda Pharmaceuticals America, Inc. GLIMEPIRIDE; PIOGLITAZONE HYDROCHLORIDE 2 mg/1; 30 mg/1 30 TABLET in 1 BOTTLE (64764-302-30)
64764-302-90 64764-302 HUMAN PRESCRIPTION DRUG Duetact pioglitazone and glimepiride TABLET ORAL 20060728 N/A NDA NDA021925 Takeda Pharmaceuticals America, Inc. GLIMEPIRIDE; PIOGLITAZONE HYDROCHLORIDE 2 mg/1; 30 mg/1 90 TABLET in 1 BOTTLE (64764-302-90)
64764-304-30 64764-304 HUMAN PRESCRIPTION DRUG Duetact pioglitazone and glimepiride TABLET ORAL 20060728 N/A NDA NDA021925 Takeda Pharmaceuticals America, Inc. GLIMEPIRIDE; PIOGLITAZONE HYDROCHLORIDE 4 mg/1; 30 mg/1 30 TABLET in 1 BOTTLE (64764-304-30)
64764-304-90 64764-304 HUMAN PRESCRIPTION DRUG Duetact pioglitazone and glimepiride TABLET ORAL 20060728 N/A NDA NDA021925 Takeda Pharmaceuticals America, Inc. GLIMEPIRIDE; PIOGLITAZONE HYDROCHLORIDE 4 mg/1; 30 mg/1 90 TABLET in 1 BOTTLE (64764-304-90)
66993-821-30 66993-821 HUMAN PRESCRIPTION DRUG pioglitazone and glimepiride pioglitazone and glimepiride TABLET ORAL 20150804 N/A NDA AUTHORIZED GENERIC NDA021925 Prasco Laboratories GLIMEPIRIDE; PIOGLITAZONE HYDROCHLORIDE 2 mg/1; 30 mg/1 30 TABLET in 1 BOTTLE (66993-821-30)
66993-822-30 66993-822 HUMAN PRESCRIPTION DRUG pioglitazone and glimepiride pioglitazone and glimepiride TABLET ORAL 20150804 N/A NDA AUTHORIZED GENERIC NDA021925 Prasco Laboratories GLIMEPIRIDE; PIOGLITAZONE HYDROCHLORIDE 4 mg/1; 30 mg/1 30 TABLET in 1 BOTTLE (66993-822-30)
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