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"
符合检索条件的记录共 294 条，共 15 页，当前第 11 页 ，可点击列名称排序
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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
76420-030-60 76420-030 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20200619 N/A ANDA ANDA208170 Asclemed USA, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (76420-030-60)
76420-030-90 76420-030 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20200619 N/A ANDA ANDA208170 Asclemed USA, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (76420-030-90)
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)
72189-545-21 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 21 TABLET, FILM COATED in 1 BOTTLE (72189-545-21)
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)
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)
72888-012-00 72888-012 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20211101 N/A ANDA ANDA208170 Advagen Pharma Limited CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (72888-012-00)
72888-012-01 72888-012 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20170531 N/A ANDA ANDA208170 Advagen Pharma Limited CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (72888-012-01)
72888-012-05 72888-012 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20170531 N/A ANDA ANDA208170 Advagen Pharma Limited CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (72888-012-05)
72888-013-01 72888-013 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20170531 N/A ANDA ANDA208170 Advagen Pharma Limited CYCLOBENZAPRINE HYDROCHLORIDE 7.5 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (72888-013-01)
72888-014-00 72888-014 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20170531 N/A ANDA ANDA208170 Advagen Pharma Limited CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (72888-014-00)
72888-014-01 72888-014 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20170531 N/A ANDA ANDA208170 Advagen Pharma Limited CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (72888-014-01)
72888-014-05 72888-014 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20170531 N/A ANDA ANDA208170 Advagen Pharma Limited CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (72888-014-05)
80425-0498-1 80425-0498 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20250320 N/A ANDA ANDA208170 Advanced Rx of Tennessee, LLC CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (80425-0498-1)
80425-0498-2 80425-0498 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20250320 N/A ANDA ANDA208170 Advanced Rx of Tennessee, LLC CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (80425-0498-2)
80425-0498-3 80425-0498 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20250320 N/A ANDA ANDA208170 Advanced Rx of Tennessee, LLC CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (80425-0498-3)
71335-2479-0 71335-2479 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20250203 N/A ANDA ANDA208170 Bryant Ranch Prepack CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (71335-2479-0)
71335-2479-1 71335-2479 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20240924 N/A ANDA ANDA208170 Bryant Ranch Prepack CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71335-2479-1)
71335-2479-2 71335-2479 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20241108 N/A ANDA ANDA208170 Bryant Ranch Prepack CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71335-2479-2)
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