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
51655-973-54	51655-973	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine	TABLET, FILM COATED	ORAL	20220824	N/A	ANDA	ANDA090478	Northwind Health Company, LLC	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-973-54)
51655-973-87	51655-973	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine	TABLET, FILM COATED	ORAL	20220504	N/A	ANDA	ANDA090478	Northwind Health Company, LLC	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-973-87)
68071-3154-1	68071-3154	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine	TABLET, FILM COATED	ORAL	20170517	N/A	ANDA	ANDA090478	NuCare Pharmaceuticals, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (68071-3154-1)
68071-3154-3	68071-3154	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine	TABLET, FILM COATED	ORAL	20170517	N/A	ANDA	ANDA090478	NuCare Pharmaceuticals, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68071-3154-3)
68071-3154-6	68071-3154	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine	TABLET, FILM COATED	ORAL	20170517	N/A	ANDA	ANDA090478	NuCare Pharmaceuticals, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	6 TABLET, FILM COATED in 1 BOTTLE (68071-3154-6)
68071-3154-7	68071-3154	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine	TABLET, FILM COATED	ORAL	20170517	N/A	ANDA	ANDA090478	NuCare Pharmaceuticals, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	7 TABLET, FILM COATED in 1 BOTTLE (68071-3154-7)