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
71335-0096-0	71335-0096	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20220309	N/A	ANDA	ANDA078722	Bryant Ranch Prepack	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (71335-0096-0)
71335-0096-1	71335-0096	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20180320	N/A	ANDA	ANDA078722	Bryant Ranch Prepack	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-0096-1)
71335-0096-2	71335-0096	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20180305	N/A	ANDA	ANDA078722	Bryant Ranch Prepack	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-0096-2)
71335-0096-3	71335-0096	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20180320	N/A	ANDA	ANDA078722	Bryant Ranch Prepack	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-0096-3)
71335-0096-4	71335-0096	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20180509	N/A	ANDA	ANDA078722	Bryant Ranch Prepack	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (71335-0096-4)
71335-0096-5	71335-0096	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20190927	N/A	ANDA	ANDA078722	Bryant Ranch Prepack	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (71335-0096-5)
71335-0096-6	71335-0096	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20220309	N/A	ANDA	ANDA078722	Bryant Ranch Prepack	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	45 TABLET, FILM COATED in 1 BOTTLE (71335-0096-6)
71335-0096-7	71335-0096	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20180904	N/A	ANDA	ANDA078722	Bryant Ranch Prepack	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	9 TABLET, FILM COATED in 1 BOTTLE (71335-0096-7)
71335-0096-8	71335-0096	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20220309	N/A	ANDA	ANDA078722	Bryant Ranch Prepack	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (71335-0096-8)
69306-075-09	69306-075	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20210115	N/A	ANDA	ANDA078722	Doc Rx	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (69306-075-09)
69420-1001-1	69420-1001	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20150325	N/A	ANDA	ANDA078722	SA3, LLC	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (69420-1001-1)
69420-1001-2	69420-1001	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20150325	N/A	ANDA	ANDA078722	SA3, LLC	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (69420-1001-2)
69420-1001-3	69420-1001	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20150325	N/A	ANDA	ANDA078722	SA3, LLC	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (69420-1001-3)
50090-1848-0	50090-1848	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20150528	N/A	ANDA	ANDA078722	A-S Medication Solutions	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (50090-1848-0)
50090-1848-1	50090-1848	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20150528	N/A	ANDA	ANDA078722	A-S Medication Solutions	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (50090-1848-1)
50090-1848-2	50090-1848	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20150528	N/A	ANDA	ANDA078722	A-S Medication Solutions	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (50090-1848-2)
55700-239-90	55700-239	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20220408	20271231	ANDA	ANDA078722	Quality Care Products LLC	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (55700-239-90)
71335-0096-9	71335-0096	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20180423	N/A	ANDA	ANDA078722	Bryant Ranch Prepack	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	14 TABLET, FILM COATED in 1 BOTTLE (71335-0096-9)
76420-010-01	76420-010	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20221021	N/A	ANDA	ANDA078722	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (76420-010-01)
76420-010-05	76420-010	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20221021	N/A	ANDA	ANDA078722	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (76420-010-05)