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
13668-692-90	13668-692	HUMAN PRESCRIPTION DRUG	TIOPRONIN	tiopronin	TABLET, DELAYED RELEASE	ORAL	20240130	N/A	ANDA	ANDA216990	Torrent Pharmaceuticals Limited	TIOPRONIN	300 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (13668-692-90)
13668-691-03	13668-691	HUMAN PRESCRIPTION DRUG	TIOPRONIN	tiopronin	TABLET, DELAYED RELEASE	ORAL	20240130	N/A	ANDA	ANDA216990	Torrent Pharmaceuticals Limited	TIOPRONIN	100 mg/1	300 TABLET, DELAYED RELEASE in 1 BOTTLE (13668-691-03)
70709-123-90	70709-123	HUMAN PRESCRIPTION DRUG	VENXXIVA	tiopronin	TABLET, DELAYED RELEASE	ORAL	20250122	N/A	ANDA	ANDA216990	Cycle Pharmaceuticals Ltd.	TIOPRONIN	300 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (70709-123-90)
70709-121-30	70709-121	HUMAN PRESCRIPTION DRUG	VENXXIVA	tiopronin	TABLET, DELAYED RELEASE	ORAL	20250122	N/A	ANDA	ANDA216990	Cycle Pharmaceuticals Ltd.	TIOPRONIN	100 mg/1	300 TABLET, DELAYED RELEASE in 1 BOTTLE (70709-121-30)