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
82804-058-30	82804-058	HUMAN PRESCRIPTION DRUG	Solifenacin succinate	solifenacin succinate	TABLET, FILM COATED	ORAL	20240115	N/A	ANDA	ANDA202551	Proficient Rx LP	SOLIFENACIN SUCCINATE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (82804-058-30)
82804-058-60	82804-058	HUMAN PRESCRIPTION DRUG	Solifenacin succinate	solifenacin succinate	TABLET, FILM COATED	ORAL	20240115	N/A	ANDA	ANDA202551	Proficient Rx LP	SOLIFENACIN SUCCINATE	10 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (82804-058-60)
82804-058-90	82804-058	HUMAN PRESCRIPTION DRUG	Solifenacin succinate	solifenacin succinate	TABLET, FILM COATED	ORAL	20240115	N/A	ANDA	ANDA202551	Proficient Rx LP	SOLIFENACIN SUCCINATE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (82804-058-90)
0591-3796-19	0591-3796	HUMAN PRESCRIPTION DRUG	Solifenacin succinate	solifenacin succinate	TABLET, FILM COATED	ORAL	20200409	N/A	ANDA	ANDA202551	Actavis Pharma, Inc.	SOLIFENACIN SUCCINATE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (0591-3796-19)
0591-3796-30	0591-3796	HUMAN PRESCRIPTION DRUG	Solifenacin succinate	solifenacin succinate	TABLET, FILM COATED	ORAL	20230123	N/A	ANDA	ANDA202551	Actavis Pharma, Inc.	SOLIFENACIN SUCCINATE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0591-3796-30)
0591-3795-19	0591-3795	HUMAN PRESCRIPTION DRUG	Solifenacin succinate	solifenacin succinate	TABLET, FILM COATED	ORAL	20200630	N/A	ANDA	ANDA202551	Actavis Pharma, Inc.	SOLIFENACIN SUCCINATE	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (0591-3795-19)
0591-3795-30	0591-3795	HUMAN PRESCRIPTION DRUG	Solifenacin succinate	solifenacin succinate	TABLET, FILM COATED	ORAL	20230123	N/A	ANDA	ANDA202551	Actavis Pharma, Inc.	SOLIFENACIN SUCCINATE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0591-3795-30)