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=ANDA204975"
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
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)
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)
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)
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