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
71335-2696-1	71335-2696	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20250924	N/A	NDA AUTHORIZED GENERIC	NDA021777	Bryant Ranch Prepack	CYCLOBENZAPRINE HYDROCHLORIDE	30 mg/1	30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-2696-1)
71335-2696-2	71335-2696	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20250924	N/A	NDA AUTHORIZED GENERIC	NDA021777	Bryant Ranch Prepack	CYCLOBENZAPRINE HYDROCHLORIDE	30 mg/1	60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-2696-2)
72189-389-60	72189-389	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine HCL ER	Cyclobenzaprine HCL ER	CAPSULE, EXTENDED RELEASE	ORAL	20221109	N/A	NDA AUTHORIZED GENERIC	NDA021777	Direct_Rx	CYCLOBENZAPRINE HYDROCHLORIDE	15 mg/1	60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72189-389-60)
0115-1437-13	0115-1437	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20190301	N/A	NDA AUTHORIZED GENERIC	NDA021777	Amneal Pharmaceuticals of New York LLC	CYCLOBENZAPRINE HYDROCHLORIDE	30 mg/1	60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0115-1437-13)
0093-1921-06	0093-1921	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20190304	N/A	NDA AUTHORIZED GENERIC	NDA021777	Teva Pharmaceuticals USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	30 mg/1	60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0093-1921-06)