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
0527-1934-09	0527-1934	HUMAN PRESCRIPTION DRUG	Solifenacin Succinate	solifenacin succinate	TABLET, FILM COATED	ORAL	20230606	N/A	ANDA	ANDA211622	Lannett Company, Inc.	SOLIFENACIN SUCCINATE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (0527-1934-09)
0527-1934-10	0527-1934	HUMAN PRESCRIPTION DRUG	Solifenacin Succinate	solifenacin succinate	TABLET, FILM COATED	ORAL	20230606	N/A	ANDA	ANDA211622	Lannett Company, Inc.	SOLIFENACIN SUCCINATE	10 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (0527-1934-10)
0527-1934-30	0527-1934	HUMAN PRESCRIPTION DRUG	Solifenacin Succinate	solifenacin succinate	TABLET, FILM COATED	ORAL	20230606	N/A	ANDA	ANDA211622	Lannett Company, Inc.	SOLIFENACIN SUCCINATE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0527-1934-30)
0527-1933-30	0527-1933	HUMAN PRESCRIPTION DRUG	Solifenacin Succinate	solifenacin succinate	TABLET, FILM COATED	ORAL	20230606	N/A	ANDA	ANDA211622	Lannett Company, Inc.	SOLIFENACIN SUCCINATE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0527-1933-30)
0527-1933-10	0527-1933	HUMAN PRESCRIPTION DRUG	Solifenacin Succinate	solifenacin succinate	TABLET, FILM COATED	ORAL	20230606	N/A	ANDA	ANDA211622	Lannett Company, Inc.	SOLIFENACIN SUCCINATE	5 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (0527-1933-10)
0527-1933-09	0527-1933	HUMAN PRESCRIPTION DRUG	Solifenacin Succinate	solifenacin succinate	TABLET, FILM COATED	ORAL	20230606	N/A	ANDA	ANDA211622	Lannett Company, Inc.	SOLIFENACIN SUCCINATE	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (0527-1933-09)