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
0178-0901-90	0178-0901	HUMAN PRESCRIPTION DRUG	Thiola EC	tiopronin	TABLET, DELAYED RELEASE	ORAL	20190628	N/A	NDA	NDA211843	Mission Pharmacal Company	TIOPRONIN	300 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (0178-0901-90)
0178-0902-01	0178-0902	HUMAN PRESCRIPTION DRUG	Thiola EC	tiopronin	TABLET, DELAYED RELEASE	ORAL	20190628	N/A	NDA	NDA211843	Mission Pharmacal Company	TIOPRONIN	100 mg/1	300 TABLET, DELAYED RELEASE in 1 BOTTLE (0178-0902-01)
44523-055-01	44523-055	HUMAN PRESCRIPTION DRUG	Tiopronin	Tiopronin	TABLET, DELAYED RELEASE	ORAL	20241205	N/A	NDA AUTHORIZED GENERIC	NDA211843	BioComp Pharma, Inc.	TIOPRONIN	300 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (44523-055-01)
44523-054-01	44523-054	HUMAN PRESCRIPTION DRUG	Tiopronin	Tiopronin	TABLET, DELAYED RELEASE	ORAL	20241205	N/A	NDA AUTHORIZED GENERIC	NDA211843	BioComp Pharma, Inc.	TIOPRONIN	100 mg/1	300 TABLET, DELAYED RELEASE in 1 BOTTLE (44523-054-01)