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
70518-3415-1 70518-3415 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20240430 N/A ANDA ANDA208170 REMEDYREPACK INC. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3415-1)
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)
50090-4727-3 50090-4727 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20191118 N/A ANDA ANDA208170 A-S Medication Solutions CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (50090-4727-3)
50090-4727-4 50090-4727 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20191118 N/A ANDA ANDA208170 A-S Medication Solutions CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (50090-4727-4)
50090-4727-6 50090-4727 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20191118 N/A ANDA ANDA208170 A-S Medication Solutions CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 7 TABLET, FILM COATED in 1 BOTTLE (50090-4727-6)
50090-4727-7 50090-4727 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20191118 N/A ANDA ANDA208170 A-S Medication Solutions CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 14 TABLET, FILM COATED in 1 BOTTLE (50090-4727-7)
50090-4727-8 50090-4727 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20191118 N/A ANDA ANDA208170 A-S Medication Solutions CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 21 TABLET, FILM COATED in 1 BOTTLE (50090-4727-8)
50090-4727-9 50090-4727 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20191118 N/A ANDA ANDA208170 A-S Medication Solutions CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (50090-4727-9)
60760-766-04 60760-766 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20230629 N/A ANDA ANDA208170 ST. MARY'S MEDICAL PARK PHARMACY CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 4 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-766-04)
60760-766-15 60760-766 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20230629 N/A ANDA ANDA208170 ST. MARY'S MEDICAL PARK PHARMACY CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-766-15)
60760-766-30 60760-766 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20170531 N/A ANDA ANDA208170 ST. MARY'S MEDICAL PARK PHARMACY CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-766-30)
67296-2084-4 67296-2084 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20170531 N/A ANDA ANDA208170 Redpharm Drug CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 21 TABLET, FILM COATED in 1 BOTTLE (67296-2084-4)
68071-3475-1 68071-3475 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20230801 N/A ANDA ANDA208170 NuCare Pharmaceuticals,Inc. CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (68071-3475-1)
68071-3475-2 68071-3475 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20230801 N/A ANDA ANDA208170 NuCare Pharmaceuticals,Inc. CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 12 TABLET, FILM COATED in 1 BOTTLE (68071-3475-2)
68071-3475-3 68071-3475 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20230801 N/A ANDA ANDA208170 NuCare Pharmaceuticals,Inc. CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68071-3475-3)
68071-3475-4 68071-3475 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20240923 N/A ANDA ANDA208170 NuCare Pharmaceuticals,Inc. CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 14 TABLET, FILM COATED in 1 BOTTLE (68071-3475-4)
68071-3475-9 68071-3475 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20250114 N/A ANDA ANDA208170 NuCare Pharmaceuticals,Inc. CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68071-3475-9)
85766-041-00 85766-041 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20250813 N/A ANDA ANDA208170 Sportpharm LLC CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (85766-041-00)
85766-041-01 85766-041 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20250813 N/A ANDA ANDA208170 Sportpharm LLC CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 1 TABLET, FILM COATED in 1 BOTTLE (85766-041-01)
85766-041-02 85766-041 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20250813 N/A ANDA ANDA208170 Sportpharm LLC CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 2 TABLET, FILM COATED in 1 BOTTLE (85766-041-02)
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