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
82461-714-90	82461-714	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20260111	N/A	ANDA	ANDA208170	Medcore LLC	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (82461-714-90)
82461-716-90	82461-716	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20260111	N/A	ANDA	ANDA208170	Medcore LLC	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (82461-716-90)
67046-1566-3	67046-1566	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20250617	N/A	ANDA	ANDA208170	Coupler LLC	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1566-3)
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)
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)
72603-312-01	72603-312	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20241101	N/A	ANDA	ANDA208170	NORTHSTAR RX LLC	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (72603-312-01)
72603-312-02	72603-312	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20241101	N/A	ANDA	ANDA208170	NORTHSTAR RX LLC	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (72603-312-02)
72603-312-03	72603-312	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20241101	N/A	ANDA	ANDA208170	NORTHSTAR RX LLC	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (72603-312-03)
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)
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)
70518-3814-0	70518-3814	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20230801	N/A	ANDA	ANDA208170	REMEDYREPACK INC.	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3814-0)
70518-3814-3	70518-3814	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20231007	N/A	ANDA	ANDA208170	REMEDYREPACK INC.	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3814-3)
70518-3814-5	70518-3814	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20231223	N/A	ANDA	ANDA208170	REMEDYREPACK INC.	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3814-5)
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)
76420-456-00	76420-456	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20250813	N/A	ANDA	ANDA208170	ASCLEMED USA INC.	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (76420-456-00)