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
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)
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)
68071-3561-4 68071-3561 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20240102 N/A ANDA ANDA208170 NuCare Pharmaceuticals,Inc. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 4 TABLET, FILM COATED in 1 BOTTLE (68071-3561-4)
68071-3561-6 68071-3561 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20240102 N/A ANDA ANDA208170 NuCare Pharmaceuticals,Inc. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 9 TABLET, FILM COATED in 1 BOTTLE (68071-3561-6)
68071-3805-1 68071-3805 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20250304 N/A ANDA ANDA208170 NuCare Pharmaceuticals, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 7.5 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (68071-3805-1)
68071-3805-7 68071-3805 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20250304 N/A ANDA ANDA208170 NuCare Pharmaceuticals, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 7.5 mg/1 21 TABLET, FILM COATED in 1 BOTTLE (68071-3805-7)
68071-3915-2 68071-3915 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20251117 N/A ANDA ANDA208170 NuCare Pharmaceuticals, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 12 TABLET, FILM COATED in 1 BOTTLE (68071-3915-2)
68071-3915-3 68071-3915 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20251203 N/A ANDA ANDA208170 NuCare Pharmaceuticals, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68071-3915-3)
68071-4655-2 68071-4655 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20181207 N/A ANDA ANDA208170 NuCare Pharmaceutuicals,Inc. CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 12 TABLET, FILM COATED in 1 BOTTLE (68071-4655-2)
68071-4655-3 68071-4655 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20181207 N/A ANDA ANDA208170 NuCare Pharmaceutuicals,Inc. CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68071-4655-3)
68071-4935-6 68071-4935 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20190621 N/A ANDA ANDA208170 NuCare Pharmaceuticals,Inc. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 6 TABLET, FILM COATED in 1 BOTTLE (68071-4935-6)
68071-4951-2 68071-4951 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20190628 N/A ANDA ANDA208170 NuCare Pharmaceuticals,Inc. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (68071-4951-2)
68071-4951-3 68071-4951 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20190628 N/A ANDA ANDA208170 NuCare Pharmaceuticals,Inc. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68071-4951-3)
68788-8471-2 68788-8471 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20230629 N/A ANDA ANDA208170 Preferred Pharmaceuticals Inc. CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (68788-8471-2)
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