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）

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
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)
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)
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)
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)