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
72189-283-15	72189-283	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	CYCLOBENZAPRINE HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20211019	N/A	ANDA	ANDA208170	DirectRx	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (72189-283-15)
72189-283-20	72189-283	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	CYCLOBENZAPRINE HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20211019	N/A	ANDA	ANDA208170	DirectRx	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (72189-283-20)
72189-283-30	72189-283	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	CYCLOBENZAPRINE HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20211019	N/A	ANDA	ANDA208170	DirectRx	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (72189-283-30)
72189-283-60	72189-283	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	CYCLOBENZAPRINE HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20211019	N/A	ANDA	ANDA208170	DirectRx	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (72189-283-60)
72189-283-82	72189-283	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	CYCLOBENZAPRINE HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20211019	N/A	ANDA	ANDA208170	DirectRx	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (72189-283-82)
72189-283-90	72189-283	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	CYCLOBENZAPRINE HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20211019	N/A	ANDA	ANDA208170	DirectRx	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (72189-283-90)
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)
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)
68071-3805-7	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	21 TABLET, FILM COATED in 1 BOTTLE (68071-3805-7)
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)
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)
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)
85766-041-00	85766-041	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20250813	N/A	ANDA	ANDA208170	Sportpharm, Inc. dba Sportpharm	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (85766-041-00)