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)
76420-828-00	76420-828	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20240702	N/A	ANDA	ANDA208170	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (76420-828-00)
76420-828-01	76420-828	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20240702	N/A	ANDA	ANDA208170	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (76420-828-01)
76420-828-05	76420-828	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20240702	N/A	ANDA	ANDA208170	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (76420-828-05)
76420-828-07	76420-828	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20250204	N/A	ANDA	ANDA208170	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	7 TABLET, FILM COATED in 1 BOTTLE (76420-828-07)
76420-828-12	76420-828	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20240702	N/A	ANDA	ANDA208170	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (76420-828-12)
76420-828-30	76420-828	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20240702	N/A	ANDA	ANDA208170	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (76420-828-30)
76420-828-60	76420-828	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20240702	N/A	ANDA	ANDA208170	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (76420-828-60)
76420-828-90	76420-828	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20240702	N/A	ANDA	ANDA208170	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (76420-828-90)
70518-2611-4	70518-2611	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20241108	N/A	ANDA	ANDA208170	REMEDYREPACK INC.	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2611-4)
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)
71205-356-21	71205-356	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20230406	N/A	ANDA	ANDA208170	Proficient Rx LP	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	21 TABLET, FILM COATED in 1 BOTTLE (71205-356-21)
71205-356-30	71205-356	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20191101	N/A	ANDA	ANDA208170	Proficient Rx LP	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71205-356-30)