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=ANDA078604"
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
76282-250-01 76282-250 HUMAN PRESCRIPTION DRUG Escitalopram oxalate escitalopram TABLET, FILM COATED ORAL 20121001 N/A ANDA ANDA078604 Exelan Pharmaceuticals Inc. ESCITALOPRAM OXALATE 10 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (76282-250-01)
76282-250-05 76282-250 HUMAN PRESCRIPTION DRUG Escitalopram oxalate escitalopram TABLET, FILM COATED ORAL 20121001 N/A ANDA ANDA078604 Exelan Pharmaceuticals Inc. ESCITALOPRAM OXALATE 10 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (76282-250-05)
76282-250-10 76282-250 HUMAN PRESCRIPTION DRUG Escitalopram oxalate escitalopram TABLET, FILM COATED ORAL 20121001 N/A ANDA ANDA078604 Exelan Pharmaceuticals Inc. ESCITALOPRAM OXALATE 10 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (76282-250-10)
76282-250-30 76282-250 HUMAN PRESCRIPTION DRUG Escitalopram oxalate escitalopram TABLET, FILM COATED ORAL 20121001 N/A ANDA ANDA078604 Exelan Pharmaceuticals Inc. ESCITALOPRAM OXALATE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (76282-250-30)
76282-250-90 76282-250 HUMAN PRESCRIPTION DRUG Escitalopram oxalate escitalopram TABLET, FILM COATED ORAL 20121001 N/A ANDA ANDA078604 Exelan Pharmaceuticals Inc. ESCITALOPRAM OXALATE 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (76282-250-90)
76282-251-01 76282-251 HUMAN PRESCRIPTION DRUG Escitalopram oxalate escitalopram TABLET, FILM COATED ORAL 20121001 N/A ANDA ANDA078604 Exelan Pharmaceuticals Inc. ESCITALOPRAM OXALATE 20 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (76282-251-01)
76282-251-05 76282-251 HUMAN PRESCRIPTION DRUG Escitalopram oxalate escitalopram TABLET, FILM COATED ORAL 20121001 N/A ANDA ANDA078604 Exelan Pharmaceuticals Inc. ESCITALOPRAM OXALATE 20 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (76282-251-05)
76282-251-10 76282-251 HUMAN PRESCRIPTION DRUG Escitalopram oxalate escitalopram TABLET, FILM COATED ORAL 20121001 N/A ANDA ANDA078604 Exelan Pharmaceuticals Inc. ESCITALOPRAM OXALATE 20 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (76282-251-10)
76282-251-30 76282-251 HUMAN PRESCRIPTION DRUG Escitalopram oxalate escitalopram TABLET, FILM COATED ORAL 20121001 N/A ANDA ANDA078604 Exelan Pharmaceuticals Inc. ESCITALOPRAM OXALATE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (76282-251-30)
76282-251-90 76282-251 HUMAN PRESCRIPTION DRUG Escitalopram oxalate escitalopram TABLET, FILM COATED ORAL 20121001 N/A ANDA ANDA078604 Exelan Pharmaceuticals Inc. ESCITALOPRAM OXALATE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (76282-251-90)
76282-249-05 76282-249 HUMAN PRESCRIPTION DRUG Escitalopram oxalate escitalopram TABLET, FILM COATED ORAL 20121001 N/A ANDA ANDA078604 Exelan Pharmaceuticals Inc. ESCITALOPRAM OXALATE 5 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (76282-249-05)
76282-249-10 76282-249 HUMAN PRESCRIPTION DRUG Escitalopram oxalate escitalopram TABLET, FILM COATED ORAL 20121001 N/A ANDA ANDA078604 Exelan Pharmaceuticals Inc. ESCITALOPRAM OXALATE 5 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (76282-249-10)
76282-249-30 76282-249 HUMAN PRESCRIPTION DRUG Escitalopram oxalate escitalopram TABLET, FILM COATED ORAL 20121001 N/A ANDA ANDA078604 Exelan Pharmaceuticals Inc. ESCITALOPRAM OXALATE 5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (76282-249-30)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase