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
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)
71335-1266-0	71335-1266	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20190711	N/A	ANDA	ANDA208170	Bryant Ranch Prepack	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	40 TABLET, FILM COATED in 1 BOTTLE (71335-1266-0)
71335-1266-1	71335-1266	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20190711	N/A	ANDA	ANDA208170	Bryant Ranch Prepack	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	14 TABLET, FILM COATED in 1 BOTTLE (71335-1266-1)
71335-1266-2	71335-1266	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20190711	N/A	ANDA	ANDA208170	Bryant Ranch Prepack	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	84 TABLET, FILM COATED in 1 BOTTLE (71335-1266-2)
71335-1266-3	71335-1266	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20190711	N/A	ANDA	ANDA208170	Bryant Ranch Prepack	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-1266-3)
71335-1266-4	71335-1266	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20190711	N/A	ANDA	ANDA208170	Bryant Ranch Prepack	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (71335-1266-4)
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)
51655-427-26	51655-427	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20210401	N/A	ANDA	ANDA208170	Northwind Health Company, LLC	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-427-26)
51655-427-52	51655-427	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20220413	N/A	ANDA	ANDA208170	Northwind Health Company, LLC	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-427-52)
51655-427-53	51655-427	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20200901	N/A	ANDA	ANDA208170	Northwind Health Company, LLC	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-427-53)
72603-310-01	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	100 TABLET, FILM COATED in 1 BOTTLE (72603-310-01)
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)
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)
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)