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
72603-414-01	72603-414	HUMAN PRESCRIPTION DRUG	FESOTERODINE FUMARATE	FESOTERODINE FUMARATE	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20240501	N/A	ANDA	ANDA204792	NorthStar RxLLC	FESOTERODINE FUMARATE	8 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72603-414-01)
72603-413-01	72603-413	HUMAN PRESCRIPTION DRUG	FESOTERODINE FUMARATE	FESOTERODINE FUMARATE	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20240501	N/A	ANDA	ANDA204792	NorthStar RxLLC	FESOTERODINE FUMARATE	4 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72603-413-01)
31722-033-90	31722-033	HUMAN PRESCRIPTION DRUG	FESOTERODINE FUMARATE	FESOTERODINE FUMARATE	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20240109	N/A	ANDA	ANDA204792	Camber Pharmaceuticals, Inc.	FESOTERODINE FUMARATE	4 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (31722-033-90)
31722-033-30	31722-033	HUMAN PRESCRIPTION DRUG	FESOTERODINE FUMARATE	FESOTERODINE FUMARATE	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20240109	N/A	ANDA	ANDA204792	Camber Pharmaceuticals, Inc.	FESOTERODINE FUMARATE	4 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (31722-033-30)
31722-034-30	31722-034	HUMAN PRESCRIPTION DRUG	FESOTERODINE FUMARATE	FESOTERODINE FUMARATE	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20240109	N/A	ANDA	ANDA204792	Camber Pharmaceuticals, Inc.	FESOTERODINE FUMARATE	8 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (31722-034-30)
31722-034-90	31722-034	HUMAN PRESCRIPTION DRUG	FESOTERODINE FUMARATE	FESOTERODINE FUMARATE	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20240109	N/A	ANDA	ANDA204792	Camber Pharmaceuticals, Inc.	FESOTERODINE FUMARATE	8 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (31722-034-90)