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=ANDA091124"
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
80425-0098-1 80425-0098 HUMAN PRESCRIPTION DRUG Eszopiclone Eszopiclone TABLET, FILM COATED ORAL 20140415 N/A ANDA ANDA091124 Advanced Rx Pharmacy of Tennessee, LLC ESZOPICLONE 1 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (80425-0098-1)
80425-0115-1 80425-0115 HUMAN PRESCRIPTION DRUG Eszopiclone Eszopiclone TABLET, FILM COATED ORAL 20140415 N/A ANDA ANDA091124 Advanced Rx Pharmacy of Tennessee, LLC ESZOPICLONE 3 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (80425-0115-1)
68180-322-01 68180-322 HUMAN PRESCRIPTION DRUG Eszopiclone Eszopiclone TABLET, FILM COATED ORAL 20140415 N/A ANDA ANDA091124 Lupin Pharmaceuticals, Inc. ESZOPICLONE 1 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (68180-322-01)
68180-323-01 68180-323 HUMAN PRESCRIPTION DRUG Eszopiclone Eszopiclone TABLET, FILM COATED ORAL 20140415 N/A ANDA ANDA091124 Lupin Pharmaceuticals, Inc. ESZOPICLONE 2 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (68180-323-01)
68180-324-01 68180-324 HUMAN PRESCRIPTION DRUG Eszopiclone Eszopiclone TABLET, FILM COATED ORAL 20140415 N/A ANDA ANDA091124 Lupin Pharmaceuticals, Inc. ESZOPICLONE 3 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (68180-324-01)
43063-795-30 43063-795 HUMAN PRESCRIPTION DRUG Eszopiclone Eszopiclone TABLET, FILM COATED ORAL 20171009 N/A ANDA ANDA091124 PD-Rx Pharmaceuticals, Inc. ESZOPICLONE 3 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-795-30)
72189-099-30 72189-099 HUMAN PRESCRIPTION DRUG ESZOPICLONE ESZOPICLONE TABLET, FILM COATED ORAL 20200610 N/A ANDA ANDA091124 DIRECT RX ESZOPICLONE 1 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (72189-099-30)
72189-099-90 72189-099 HUMAN PRESCRIPTION DRUG ESZOPICLONE ESZOPICLONE TABLET, FILM COATED ORAL 20200610 N/A ANDA ANDA091124 DIRECT RX ESZOPICLONE 1 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (72189-099-90)
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