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）
检索条件:" 注册申请号=NDA022030"
符合检索条件的记录共 4 条，共 1 页，当前第 1 页 ，可点击列名称排序
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
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)
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
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