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
72189-080-10	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	10 TABLET, FILM COATED in 1 BOTTLE (72189-080-10)
72189-080-15	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	15 TABLET, FILM COATED in 1 BOTTLE (72189-080-15)
72189-080-20	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	20 TABLET, FILM COATED in 1 BOTTLE (72189-080-20)
72189-080-21	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	21 TABLET, FILM COATED in 1 BOTTLE (72189-080-21)
72189-080-30	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	30 TABLET, FILM COATED in 1 BOTTLE (72189-080-30)
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)
85766-003-00	85766-003	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20250620	N/A	ANDA	ANDA208170	Sportpharm LLC	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (85766-003-00)
85766-003-01	85766-003	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20250620	N/A	ANDA	ANDA208170	Sportpharm LLC	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	1 TABLET, FILM COATED in 1 BOTTLE (85766-003-01)
85766-003-02	85766-003	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20250620	N/A	ANDA	ANDA208170	Sportpharm LLC	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	2 TABLET, FILM COATED in 1 BOTTLE (85766-003-02)
85766-003-04	85766-003	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20250620	N/A	ANDA	ANDA208170	Sportpharm LLC	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	4 TABLET, FILM COATED in 1 BOTTLE (85766-003-04)
85766-003-05	85766-003	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20250620	N/A	ANDA	ANDA208170	Sportpharm LLC	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	5 TABLET, FILM COATED in 1 BOTTLE (85766-003-05)
85766-003-07	85766-003	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20250620	N/A	ANDA	ANDA208170	Sportpharm LLC	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	7 TABLET, FILM COATED in 1 BOTTLE (85766-003-07)
85766-003-10	85766-003	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20250620	N/A	ANDA	ANDA208170	Sportpharm LLC	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (85766-003-10)
85766-003-20	85766-003	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20250620	N/A	ANDA	ANDA208170	Sportpharm LLC	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (85766-003-20)
85766-003-30	85766-003	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20250620	N/A	ANDA	ANDA208170	Sportpharm LLC	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (85766-003-30)
85766-003-50	85766-003	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20250620	N/A	ANDA	ANDA208170	Sportpharm LLC	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (85766-003-50)
85766-003-60	85766-003	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20250620	N/A	ANDA	ANDA208170	Sportpharm LLC	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (85766-003-60)