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
72603-310-02 72603-310 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20241101 N/A ANDA ANDA208170 NORTHSTAR RX LLC CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (72603-310-02)
76420-030-01 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/1 100 TABLET, FILM COATED in 1 BOTTLE (76420-030-01)
76420-030-05 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/1 500 TABLET, FILM COATED in 1 BOTTLE (76420-030-05)
76420-030-12 76420-030 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20220729 N/A ANDA ANDA208170 Asclemed USA, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (76420-030-12)
76420-030-30 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 30 TABLET, FILM COATED in 1 BOTTLE (76420-030-30)
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)
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)
72603-311-01 72603-311 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20241101 N/A ANDA ANDA208170 NORTHSTAR RX LLC CYCLOBENZAPRINE HYDROCHLORIDE 7.5 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (72603-311-01)
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)
76420-265-30 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 30 TABLET, FILM COATED in 1 BOTTLE (76420-265-30)
76420-265-60 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 60 TABLET, FILM COATED in 1 BOTTLE (76420-265-60)
76420-265-90 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 90 TABLET, FILM COATED in 1 BOTTLE (76420-265-90)
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)
52817-331-10 52817-331 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20170531 N/A ANDA ANDA208170 TruPharma LLC CYCLOBENZAPRINE HYDROCHLORIDE 7.5 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (52817-331-10)
71205-065-10 71205-065 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20180702 N/A ANDA ANDA208170 Proficient Rx LP CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (71205-065-10)
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)
51655-592-20 51655-592 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20230131 N/A ANDA ANDA208170 Northwind Health Company, LLC CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-592-20)
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