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
16571-127-01	16571-127	HUMAN PRESCRIPTION DRUG	Tolterodine Tartrate	Tolterodine Tartrate	TABLET, FILM COATED	ORAL	20200124	N/A	ANDA	ANDA204721	Rising Pharma Holdings, Inc.	TOLTERODINE TARTRATE	2 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (16571-127-01)
16571-127-06	16571-127	HUMAN PRESCRIPTION DRUG	Tolterodine Tartrate	Tolterodine Tartrate	TABLET, FILM COATED	ORAL	20200124	N/A	ANDA	ANDA204721	Rising Pharma Holdings, Inc.	TOLTERODINE TARTRATE	2 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (16571-127-06)
16571-127-50	16571-127	HUMAN PRESCRIPTION DRUG	Tolterodine Tartrate	Tolterodine Tartrate	TABLET, FILM COATED	ORAL	20200124	N/A	ANDA	ANDA204721	Rising Pharma Holdings, Inc.	TOLTERODINE TARTRATE	2 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (16571-127-50)
16571-126-01	16571-126	HUMAN PRESCRIPTION DRUG	Tolterodine Tartrate	Tolterodine Tartrate	TABLET, FILM COATED	ORAL	20200124	N/A	ANDA	ANDA204721	Rising Pharma Holdings, Inc.	TOLTERODINE TARTRATE	1 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (16571-126-01)
16571-126-06	16571-126	HUMAN PRESCRIPTION DRUG	Tolterodine Tartrate	Tolterodine Tartrate	TABLET, FILM COATED	ORAL	20200124	N/A	ANDA	ANDA204721	Rising Pharma Holdings, Inc.	TOLTERODINE TARTRATE	1 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (16571-126-06)
16571-126-50	16571-126	HUMAN PRESCRIPTION DRUG	Tolterodine Tartrate	Tolterodine Tartrate	TABLET, FILM COATED	ORAL	20200124	N/A	ANDA	ANDA204721	Rising Pharma Holdings, Inc.	TOLTERODINE TARTRATE	1 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (16571-126-50)