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=NDA021777"
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
72189-362-60 72189-362 HUMAN PRESCRIPTION DRUG Cyclobenzaprine HCL ER Cyclobenzaprine HCL ER CAPSULE, EXTENDED RELEASE ORAL 20220725 N/A NDA NDA021777 Direct_Rx CYCLOBENZAPRINE HYDROCHLORIDE 15 mg/1 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72189-362-60)
72189-389-60 72189-389 HUMAN PRESCRIPTION DRUG Cyclobenzaprine HCL ER Cyclobenzaprine HCL ER CAPSULE, EXTENDED RELEASE ORAL 20221109 N/A NDA AUTHORIZED GENERIC NDA021777 Direct_Rx CYCLOBENZAPRINE HYDROCHLORIDE 15 mg/1 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72189-389-60)
63459-700-60 63459-700 HUMAN PRESCRIPTION DRUG AMRIX Cyclobenzaprine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20071002 N/A NDA NDA021777 Cephalon, LLC CYCLOBENZAPRINE HYDROCHLORIDE 15 mg/1 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63459-700-60)
71335-2696-2 71335-2696 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20250924 N/A NDA AUTHORIZED GENERIC NDA021777 Bryant Ranch Prepack CYCLOBENZAPRINE HYDROCHLORIDE 30 mg/1 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-2696-2)
71335-2696-1 71335-2696 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20250924 N/A NDA AUTHORIZED GENERIC NDA021777 Bryant Ranch Prepack CYCLOBENZAPRINE HYDROCHLORIDE 30 mg/1 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-2696-1)
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