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
59762-0800-6	59762-0800	HUMAN PRESCRIPTION DRUG	Tolterodine Tartrate	Tolterodine Tartrate	TABLET, FILM COATED	ORAL	20140121	N/A	NDA AUTHORIZED GENERIC	NDA020771	Greenstone LLC	TOLTERODINE TARTRATE	2 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (59762-0800-6)
59762-0800-2	59762-0800	HUMAN PRESCRIPTION DRUG	Tolterodine Tartrate	Tolterodine Tartrate	TABLET, FILM COATED	ORAL	20140121	N/A	NDA AUTHORIZED GENERIC	NDA020771	Greenstone LLC	TOLTERODINE TARTRATE	2 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (59762-0800-2)
59762-0170-6	59762-0170	HUMAN PRESCRIPTION DRUG	Tolterodine Tartrate	Tolterodine Tartrate	TABLET, FILM COATED	ORAL	20140121	N/A	NDA AUTHORIZED GENERIC	NDA020771	Greenstone LLC	TOLTERODINE TARTRATE	1 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (59762-0170-6)
59762-0170-1	59762-0170	HUMAN PRESCRIPTION DRUG	Tolterodine Tartrate	Tolterodine Tartrate	TABLET, FILM COATED	ORAL	20140121	N/A	NDA AUTHORIZED GENERIC	NDA020771	Greenstone LLC	TOLTERODINE TARTRATE	1 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (59762-0170-1)
0009-4541-02	0009-4541	HUMAN PRESCRIPTION DRUG	Detrol	tolterodine tartrate	TABLET, FILM COATED	ORAL	19980325	N/A	NDA	NDA020771	PHARMACIA & UPJOHN COMPANY LLC	TOLTERODINE TARTRATE	1 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (0009-4541-02)
0009-4544-02	0009-4544	HUMAN PRESCRIPTION DRUG	Detrol	tolterodine tartrate	TABLET, FILM COATED	ORAL	19980325	N/A	NDA	NDA020771	PHARMACIA & UPJOHN COMPANY LLC	TOLTERODINE TARTRATE	2 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (0009-4544-02)