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
70518-4519-0	70518-4519	HUMAN PRESCRIPTION DRUG	PIOGLITAZONE HYDROCHLORIDE	pioglitazone hydrochloride	TABLET	ORAL	20251114	N/A	ANDA	ANDA200268	REMEDYREPACK INC.	PIOGLITAZONE HYDROCHLORIDE	45 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (70518-4519-0)
71335-9664-1	71335-9664	HUMAN PRESCRIPTION DRUG	PIOGLITAZONE HYDROCHLORIDE	pioglitazone hydrochloride	TABLET	ORAL	20250627	N/A	ANDA	ANDA200268	Bryant Ranch Prepack	PIOGLITAZONE HYDROCHLORIDE	30 mg/1	30 TABLET in 1 BOTTLE (71335-9664-1)
71335-9664-2	71335-9664	HUMAN PRESCRIPTION DRUG	PIOGLITAZONE HYDROCHLORIDE	pioglitazone hydrochloride	TABLET	ORAL	20250627	N/A	ANDA	ANDA200268	Bryant Ranch Prepack	PIOGLITAZONE HYDROCHLORIDE	30 mg/1	60 TABLET in 1 BOTTLE (71335-9664-2)
71335-9664-3	71335-9664	HUMAN PRESCRIPTION DRUG	PIOGLITAZONE HYDROCHLORIDE	pioglitazone hydrochloride	TABLET	ORAL	20230306	N/A	ANDA	ANDA200268	Bryant Ranch Prepack	PIOGLITAZONE HYDROCHLORIDE	30 mg/1	90 TABLET in 1 BOTTLE (71335-9664-3)
71335-9664-4	71335-9664	HUMAN PRESCRIPTION DRUG	PIOGLITAZONE HYDROCHLORIDE	pioglitazone hydrochloride	TABLET	ORAL	20250627	N/A	ANDA	ANDA200268	Bryant Ranch Prepack	PIOGLITAZONE HYDROCHLORIDE	30 mg/1	180 TABLET in 1 BOTTLE (71335-9664-4)
72189-105-90	72189-105	HUMAN PRESCRIPTION DRUG	PIOGLITAZONE	PIOGLITAZONE	TABLET	ORAL	20200612	N/A	ANDA	ANDA200268	DIRECT RX	PIOGLITAZONE HYDROCHLORIDE	30 mg/1	90 TABLET in 1 BOTTLE (72189-105-90)