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
63539-242-77	63539-242	HUMAN PRESCRIPTION DRUG	Toviaz	fesoterodine fumarate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20210503	N/A	NDA	NDA022030	U.S. Pharmaceuticals	FESOTERODINE FUMARATE	4 mg/1	1 BLISTER PACK in 1 CARTON (63539-242-77) / 7 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
63539-183-77	63539-183	HUMAN PRESCRIPTION DRUG	Toviaz	fesoterodine fumarate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20210301	N/A	NDA	NDA022030	U.S. Pharmaceuticals	FESOTERODINE FUMARATE	8 mg/1	1 BLISTER PACK in 1 CARTON (63539-183-77) / 7 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
0069-0244-30	0069-0244	HUMAN PRESCRIPTION DRUG	Toviaz	fesoterodine fumarate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20081031	N/A	NDA	NDA022030	Pfizer Laboratories Div Pfizer Inc	FESOTERODINE FUMARATE	8 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0069-0244-30)
0069-0242-30	0069-0242	HUMAN PRESCRIPTION DRUG	Toviaz	fesoterodine fumarate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20081031	N/A	NDA	NDA022030	Pfizer Laboratories Div Pfizer Inc	FESOTERODINE FUMARATE	4 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0069-0242-30)