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 292 条，共 15 页，当前第 3 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
68788-8474-5 68788-8474 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20230701 N/A ANDA ANDA208170 Preferred Pharmaceuticals Inc. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (68788-8474-5)
68788-8474-6 68788-8474 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20230701 N/A ANDA ANDA208170 Preferred Pharmaceuticals Inc. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68788-8474-6)
68788-8474-9 68788-8474 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20230701 N/A ANDA ANDA208170 Preferred Pharmaceuticals Inc. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68788-8474-9)
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)
85766-041-03 85766-041 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20260403 N/A ANDA ANDA208170 Sportpharm LLC CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 3 TABLET, FILM COATED in 1 BOTTLE (85766-041-03)
85766-041-04 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 4 TABLET, FILM COATED in 1 BOTTLE (85766-041-04)
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)
85766-041-09 85766-041 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20260403 N/A ANDA ANDA208170 Sportpharm LLC CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (85766-041-09)
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)
50090-4722-0 50090-4722 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20191115 N/A ANDA ANDA208170 A-S Medication Solutions CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (50090-4722-0)
82804-259-30 82804-259 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20251230 N/A ANDA ANDA208170 Proficient Rx LP CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (82804-259-30)
82804-259-60 82804-259 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20251230 N/A ANDA ANDA208170 Proficient Rx LP CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (82804-259-60)
82804-259-90 82804-259 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20251230 N/A ANDA ANDA208170 Proficient Rx LP CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (82804-259-90)
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)
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