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
69306-872-06	69306-872	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20251031	N/A	ANDA	ANDA077563	Doc Rx	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (69306-872-06)
80425-0017-1	80425-0017	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine HCL	Cyclobenzaprine HCL	TABLET, FILM COATED	ORAL	20060404	N/A	ANDA	ANDA077563	Advanced Rx of Tennessee, LLC	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (80425-0017-1)
67046-1645-3	67046-1645	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20260107	N/A	ANDA	ANDA077563	Coupler LLC	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1645-3)
42291-154-60	42291-154	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20200403	N/A	ANDA	ANDA077563	AvKARE	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (42291-154-60)
42291-154-90	42291-154	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20200403	N/A	ANDA	ANDA077563	AvKARE	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (42291-154-90)
71610-907-45	71610-907	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20250508	N/A	ANDA	ANDA077563	Aphena Pharma Solutions - Tennessee, LLC	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	45 TABLET, FILM COATED in 1 BOTTLE (71610-907-45)
71610-907-53	71610-907	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20250613	N/A	ANDA	ANDA077563	Aphena Pharma Solutions - Tennessee, LLC	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71610-907-53)