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
0093-0010-06	0093-0010	HUMAN PRESCRIPTION DRUG	Tolterodine Tartrate	Tolterodine Tartrate	TABLET, FILM COATED	ORAL	20151101	N/A	ANDA	ANDA077006	Teva Pharmaceuticals USA, Inc.	TOLTERODINE TARTRATE	1 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (0093-0010-06)
0093-0018-06	0093-0018	HUMAN PRESCRIPTION DRUG	Tolterodine Tartrate	Tolterodine Tartrate	TABLET, FILM COATED	ORAL	20151101	N/A	ANDA	ANDA077006	Teva Pharmaceuticals USA, Inc.	TOLTERODINE TARTRATE	2 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (0093-0018-06)
0093-0018-05	0093-0018	HUMAN PRESCRIPTION DRUG	Tolterodine Tartrate	Tolterodine Tartrate	TABLET, FILM COATED	ORAL	20151101	N/A	ANDA	ANDA077006	Teva Pharmaceuticals USA, Inc.	TOLTERODINE TARTRATE	2 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (0093-0018-05)
71205-319-60	71205-319	HUMAN PRESCRIPTION DRUG	Tolterodine Tartrate	Tolterodine Tartrate	TABLET, FILM COATED	ORAL	20190901	N/A	ANDA	ANDA077006	Proficient Rx LP	TOLTERODINE TARTRATE	1 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71205-319-60)
71205-319-30	71205-319	HUMAN PRESCRIPTION DRUG	Tolterodine Tartrate	Tolterodine Tartrate	TABLET, FILM COATED	ORAL	20190901	N/A	ANDA	ANDA077006	Proficient Rx LP	TOLTERODINE TARTRATE	1 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71205-319-30)
71205-319-90	71205-319	HUMAN PRESCRIPTION DRUG	Tolterodine Tartrate	Tolterodine Tartrate	TABLET, FILM COATED	ORAL	20190901	N/A	ANDA	ANDA077006	Proficient Rx LP	TOLTERODINE TARTRATE	1 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71205-319-90)