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 4 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
85766-041-05 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 5 TABLET, FILM COATED in 1 BOTTLE (85766-041-05)
85766-041-07 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 7 TABLET, FILM COATED in 1 BOTTLE (85766-041-07)
85766-041-10 85766-041 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20250813 N/A ANDA ANDA208170 Sportpharm LLC CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (85766-041-10)
85766-041-14 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 14 TABLET, FILM COATED in 1 BOTTLE (85766-041-14)
85766-041-15 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 15 TABLET, FILM COATED in 1 BOTTLE (85766-041-15)
85766-041-20 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 20 TABLET, FILM COATED in 1 BOTTLE (85766-041-20)
85766-041-30 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 30 TABLET, FILM COATED in 1 BOTTLE (85766-041-30)
85766-041-50 85766-041 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20250813 N/A ANDA ANDA208170 Sportpharm LLC CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (85766-041-50)
85766-041-60 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 60 TABLET, FILM COATED in 1 BOTTLE (85766-041-60)
85766-041-90 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 90 TABLET, FILM COATED in 1 BOTTLE (85766-041-90)
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)
68071-3462-2 68071-3462 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20230719 N/A ANDA ANDA208170 NuCare Pharmaceuticals,Inc. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (68071-3462-2)
68071-3462-3 68071-3462 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20230731 N/A ANDA ANDA208170 NuCare Pharmaceuticals,Inc. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68071-3462-3)
68071-3462-5 68071-3462 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20230719 N/A ANDA ANDA208170 NuCare Pharmaceuticals,Inc. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (68071-3462-5)
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)
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