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
59746-735-01	59746-735	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20171009	N/A	ANDA	ANDA077563	Jubilant Cadista Pharmaceuticals Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (59746-735-01)
59746-735-10	59746-735	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20171009	N/A	ANDA	ANDA077563	Jubilant Cadista Pharmaceuticals Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (59746-735-10)
59746-735-30	59746-735	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20171009	N/A	ANDA	ANDA077563	Jubilant Cadista Pharmaceuticals Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (59746-735-30)
63629-2424-1	63629-2424	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20210225	N/A	ANDA	ANDA077563	Bryant Ranch Prepack	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (63629-2424-1)
80425-0547-2	80425-0547	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20250808	N/A	ANDA	ANDA077563	Advanced Rx of Tennessee, LLC	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (80425-0547-2)
80425-0547-3	80425-0547	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20250808	N/A	ANDA	ANDA077563	Advanced Rx of Tennessee, LLC	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (80425-0547-3)
80425-0547-1	80425-0547	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20250808	N/A	ANDA	ANDA077563	Advanced Rx of Tennessee, LLC	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (80425-0547-1)