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
43598-247-30	43598-247	HUMAN PRESCRIPTION DRUG	Fesoterodine fumarate	Fesoterodine fumarate	TABLET, EXTENDED RELEASE	ORAL	20220610	N/A	ANDA	ANDA204975	Dr.Reddy's Laboratories Inc.,	FESOTERODINE FUMARATE	4 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (43598-247-30)
43598-247-90	43598-247	HUMAN PRESCRIPTION DRUG	Fesoterodine fumarate	Fesoterodine fumarate	TABLET, EXTENDED RELEASE	ORAL	20220610	N/A	ANDA	ANDA204975	Dr.Reddy's Laboratories Inc.,	FESOTERODINE FUMARATE	4 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (43598-247-90)
43598-248-30	43598-248	HUMAN PRESCRIPTION DRUG	Fesoterodine fumarate	Fesoterodine fumarate	TABLET, EXTENDED RELEASE	ORAL	20220610	N/A	ANDA	ANDA204975	Dr.Reddy's Laboratories Inc.,	FESOTERODINE FUMARATE	8 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (43598-248-30)
43598-248-90	43598-248	HUMAN PRESCRIPTION DRUG	Fesoterodine fumarate	Fesoterodine fumarate	TABLET, EXTENDED RELEASE	ORAL	20220610	N/A	ANDA	ANDA204975	Dr.Reddy's Laboratories Inc.,	FESOTERODINE FUMARATE	8 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (43598-248-90)
51407-662-30	51407-662	HUMAN PRESCRIPTION DRUG	Fesoterodine fumarate	Fesoterodine fumarate	TABLET, EXTENDED RELEASE	ORAL	20220707	N/A	ANDA	ANDA204975	Golden State Medical Supply, Inc.	FESOTERODINE FUMARATE	8 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (51407-662-30)
51407-661-30	51407-661	HUMAN PRESCRIPTION DRUG	Fesoterodine fumarate	Fesoterodine fumarate	TABLET, EXTENDED RELEASE	ORAL	20220707	N/A	ANDA	ANDA204975	Golden State Medical Supply, Inc.	FESOTERODINE FUMARATE	4 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (51407-661-30)