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
68788-8706-2	68788-8706	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine hydrochloride	Cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20240701	N/A	ANDA	ANDA213324	Preferred Pharmaceuticals Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (68788-8706-2)
68788-8706-3	68788-8706	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine hydrochloride	Cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20240701	N/A	ANDA	ANDA213324	Preferred Pharmaceuticals Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68788-8706-3)
68788-8706-6	68788-8706	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine hydrochloride	Cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20240701	N/A	ANDA	ANDA213324	Preferred Pharmaceuticals Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (68788-8706-6)
68788-8706-8	68788-8706	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine hydrochloride	Cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20240701	N/A	ANDA	ANDA213324	Preferred Pharmaceuticals Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (68788-8706-8)
68788-8706-9	68788-8706	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine hydrochloride	Cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20240701	N/A	ANDA	ANDA213324	Preferred Pharmaceuticals Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68788-8706-9)