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
50090-4729-0	50090-4729	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20191118	N/A	ANDA	ANDA208170	A-S Medication Solutions	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	3 TABLET, FILM COATED in 1 BOTTLE (50090-4729-0)
50090-4729-1	50090-4729	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20191118	N/A	ANDA	ANDA208170	A-S Medication Solutions	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	12 TABLET, FILM COATED in 1 BOTTLE (50090-4729-1)
50090-4729-4	50090-4729	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20191118	N/A	ANDA	ANDA208170	A-S Medication Solutions	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	42 TABLET, FILM COATED in 1 BOTTLE (50090-4729-4)
50090-4729-8	50090-4729	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20191118	N/A	ANDA	ANDA208170	A-S Medication Solutions	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	6 TABLET, FILM COATED in 1 BOTTLE (50090-4729-8)
67046-1110-3	67046-1110	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20260423	N/A	ANDA	ANDA208170	Coupler LLC	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1110-3)
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)
50090-4727-0	50090-4727	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20191118	N/A	ANDA	ANDA208170	A-S Medication Solutions	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (50090-4727-0)
50090-4727-1	50090-4727	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20191118	N/A	ANDA	ANDA208170	A-S Medication Solutions	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (50090-4727-1)
50090-4727-2	50090-4727	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20191118	N/A	ANDA	ANDA208170	A-S Medication Solutions	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (50090-4727-2)
50090-4727-3	50090-4727	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20191118	N/A	ANDA	ANDA208170	A-S Medication Solutions	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (50090-4727-3)
50090-4727-4	50090-4727	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20191118	N/A	ANDA	ANDA208170	A-S Medication Solutions	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (50090-4727-4)
50090-4727-6	50090-4727	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20191118	N/A	ANDA	ANDA208170	A-S Medication Solutions	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	7 TABLET, FILM COATED in 1 BOTTLE (50090-4727-6)
50090-4727-7	50090-4727	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20191118	N/A	ANDA	ANDA208170	A-S Medication Solutions	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	14 TABLET, FILM COATED in 1 BOTTLE (50090-4727-7)
50090-4727-8	50090-4727	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20191118	N/A	ANDA	ANDA208170	A-S Medication Solutions	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	21 TABLET, FILM COATED in 1 BOTTLE (50090-4727-8)
50090-4727-9	50090-4727	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20191118	N/A	ANDA	ANDA208170	A-S Medication Solutions	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (50090-4727-9)
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)
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)