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=ANDA208170"
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
76420-265-10 76420-265 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20220901 N/A ANDA ANDA208170 Asclemed USA, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 7.5 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (76420-265-10)
76420-265-30 76420-265 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20220901 N/A ANDA ANDA208170 Asclemed USA, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 7.5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (76420-265-30)
76420-265-60 76420-265 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20220901 N/A ANDA ANDA208170 Asclemed USA, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 7.5 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (76420-265-60)
76420-265-90 76420-265 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20220901 N/A ANDA ANDA208170 Asclemed USA, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 7.5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (76420-265-90)
71335-1266-0 71335-1266 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20190711 N/A ANDA ANDA208170 Bryant Ranch Prepack CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 40 TABLET, FILM COATED in 1 BOTTLE (71335-1266-0)
71335-1266-1 71335-1266 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20190711 N/A ANDA ANDA208170 Bryant Ranch Prepack CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 14 TABLET, FILM COATED in 1 BOTTLE (71335-1266-1)
71335-1266-2 71335-1266 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20190711 N/A ANDA ANDA208170 Bryant Ranch Prepack CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 84 TABLET, FILM COATED in 1 BOTTLE (71335-1266-2)
71335-1266-3 71335-1266 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20190711 N/A ANDA ANDA208170 Bryant Ranch Prepack CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71335-1266-3)
71335-1266-4 71335-1266 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20190711 N/A ANDA ANDA208170 Bryant Ranch Prepack CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (71335-1266-4)
71335-1266-5 71335-1266 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20190711 N/A ANDA ANDA208170 Bryant Ranch Prepack CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (71335-1266-5)
71335-1266-6 71335-1266 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20190711 N/A ANDA ANDA208170 Bryant Ranch Prepack CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71335-1266-6)
71335-1266-7 71335-1266 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20190711 N/A ANDA ANDA208170 Bryant Ranch Prepack CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71335-1266-7)
71335-1266-8 71335-1266 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20190711 N/A ANDA ANDA208170 Bryant Ranch Prepack CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 56 TABLET, FILM COATED in 1 BOTTLE (71335-1266-8)
71335-1266-9 71335-1266 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20190711 N/A ANDA ANDA208170 Bryant Ranch Prepack CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (71335-1266-9)
72189-545-60 72189-545 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20240409 N/A ANDA ANDA208170 Direct_Rx CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (72189-545-60)
72189-545-90 72189-545 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20240409 N/A ANDA ANDA208170 Direct_Rx CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (72189-545-90)
72189-545-15 72189-545 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20240409 N/A ANDA ANDA208170 Direct_Rx CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (72189-545-15)
72189-545-30 72189-545 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20240409 N/A ANDA ANDA208170 Direct_Rx CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (72189-545-30)
50090-6864-0 50090-6864 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20231204 N/A ANDA ANDA208170 A-S Medication Solutions CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-6864-0)
76420-378-20 76420-378 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20250620 N/A ANDA ANDA208170 ASCLEMED USA INC. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (76420-378-20)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase