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
72189-545-15	72189-545	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20240409	N/A	ANDA	ANDA208170	Direct_Rx	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (72189-545-15)
72189-545-30	72189-545	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20240409	N/A	ANDA	ANDA208170	Direct_Rx	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (72189-545-30)
72189-545-60	72189-545	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20240409	N/A	ANDA	ANDA208170	Direct_Rx	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (72189-545-60)
72189-545-90	72189-545	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20240409	N/A	ANDA	ANDA208170	Direct_Rx	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (72189-545-90)
76420-378-00	76420-378	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20250620	N/A	ANDA	ANDA208170	ASCLEMED USA INC.	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (76420-378-00)
76420-378-01	76420-378	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20250620	N/A	ANDA	ANDA208170	ASCLEMED USA INC.	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	1 TABLET, FILM COATED in 1 BOTTLE (76420-378-01)
76420-378-02	76420-378	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20250620	N/A	ANDA	ANDA208170	ASCLEMED USA INC.	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	2 TABLET, FILM COATED in 1 BOTTLE (76420-378-02)
76420-378-04	76420-378	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20250620	N/A	ANDA	ANDA208170	ASCLEMED USA INC.	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	4 TABLET, FILM COATED in 1 BOTTLE (76420-378-04)
76420-378-05	76420-378	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20250620	N/A	ANDA	ANDA208170	ASCLEMED USA INC.	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	5 TABLET, FILM COATED in 1 BOTTLE (76420-378-05)
80425-0498-1	80425-0498	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20250320	N/A	ANDA	ANDA208170	Advanced Rx of Tennessee, LLC	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (80425-0498-1)
80425-0498-2	80425-0498	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20250320	N/A	ANDA	ANDA208170	Advanced Rx of Tennessee, LLC	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (80425-0498-2)
80425-0498-3	80425-0498	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20250320	N/A	ANDA	ANDA208170	Advanced Rx of Tennessee, LLC	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (80425-0498-3)
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)
67296-1621-1	67296-1621	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20180101	N/A	ANDA	ANDA208170	RedPharm Drug, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (67296-1621-1)
67296-1621-3	67296-1621	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20180101	N/A	ANDA	ANDA208170	RedPharm Drug, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (67296-1621-3)
67296-1621-5	67296-1621	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20180101	N/A	ANDA	ANDA208170	RedPharm Drug, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	5 TABLET, FILM COATED in 1 BOTTLE (67296-1621-5)
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)