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）

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
72189-080-45	72189-080	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	CYCLOBENZAPRINE HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20200513	N/A	ANDA	ANDA208170	DIRECT RX	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	45 TABLET, FILM COATED in 1 BOTTLE (72189-080-45)
72189-080-60	72189-080	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	CYCLOBENZAPRINE HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20200513	N/A	ANDA	ANDA208170	DIRECT RX	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (72189-080-60)
72189-080-72	72189-080	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	CYCLOBENZAPRINE HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20200513	N/A	ANDA	ANDA208170	DIRECT RX	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (72189-080-72)
72189-080-90	72189-080	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	CYCLOBENZAPRINE HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20200513	N/A	ANDA	ANDA208170	DIRECT RX	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (72189-080-90)
71335-2686-1	71335-2686	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20250918	N/A	ANDA	ANDA208170	Bryant Ranch Prepack	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	5 TABLET, FILM COATED in 1 BOTTLE (71335-2686-1)
71335-2686-2	71335-2686	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20250918	N/A	ANDA	ANDA208170	Bryant Ranch Prepack	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (71335-2686-2)
71335-2686-3	71335-2686	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20250918	N/A	ANDA	ANDA208170	Bryant Ranch Prepack	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	21 TABLET, FILM COATED in 1 BOTTLE (71335-2686-3)
80425-0016-1	80425-0016	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine HCL	Cyclobenzaprine HCL	TABLET, FILM COATED	ORAL	20170531	N/A	ANDA	ANDA208170	Advanced Rx of Tennessee, LLC	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (80425-0016-1)
80425-0016-2	80425-0016	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine HCL	Cyclobenzaprine HCL	TABLET, FILM COATED	ORAL	20170531	N/A	ANDA	ANDA208170	Advanced Rx of Tennessee, LLC	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (80425-0016-2)
80425-0016-3	80425-0016	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine HCL	Cyclobenzaprine HCL	TABLET, FILM COATED	ORAL	20170531	N/A	ANDA	ANDA208170	Advanced Rx of Tennessee, LLC	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (80425-0016-3)
80425-0016-4	80425-0016	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine HCL	Cyclobenzaprine HCL	TABLET, FILM COATED	ORAL	20170531	N/A	ANDA	ANDA208170	Advanced Rx of Tennessee, LLC	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (80425-0016-4)
80425-0018-1	80425-0018	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine HCL	Cyclobenzaprine HCL	TABLET, FILM COATED	ORAL	20170531	N/A	ANDA	ANDA208170	Advanced Rx of Tennessee, LLC	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (80425-0018-1)
80425-0018-2	80425-0018	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine HCL	Cyclobenzaprine HCL	TABLET, FILM COATED	ORAL	20170531	N/A	ANDA	ANDA208170	Advanced Rx of Tennessee, LLC	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (80425-0018-2)
80425-0018-3	80425-0018	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine HCL	Cyclobenzaprine HCL	TABLET, FILM COATED	ORAL	20170531	N/A	ANDA	ANDA208170	Advanced Rx of Tennessee, LLC	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (80425-0018-3)