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
76420-269-15	76420-269	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20220903	N/A	ANDA	ANDA071611	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (76420-269-15)
76420-269-20	76420-269	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20220903	N/A	ANDA	ANDA071611	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (76420-269-20)
76420-269-30	76420-269	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20220903	N/A	ANDA	ANDA071611	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (76420-269-30)
76420-269-60	76420-269	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20220903	N/A	ANDA	ANDA071611	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (76420-269-60)
76420-269-90	76420-269	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20220903	N/A	ANDA	ANDA071611	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (76420-269-90)
76420-271-07	76420-271	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20220903	N/A	ANDA	ANDA071611	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	7 TABLET, FILM COATED in 1 BOTTLE (76420-271-07)
76420-271-10	76420-271	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20220903	N/A	ANDA	ANDA071611	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (76420-271-10)
76420-271-12	76420-271	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20220903	N/A	ANDA	ANDA071611	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (76420-271-12)
76420-271-15	76420-271	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20220903	N/A	ANDA	ANDA071611	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (76420-271-15)
76420-271-20	76420-271	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20220903	N/A	ANDA	ANDA071611	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (76420-271-20)
76420-271-30	76420-271	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20220903	N/A	ANDA	ANDA071611	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (76420-271-30)
76420-271-60	76420-271	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20220903	N/A	ANDA	ANDA071611	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (76420-271-60)
76420-271-90	76420-271	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20220903	N/A	ANDA	ANDA071611	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (76420-271-90)
76420-271-01	76420-271	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20220903	N/A	ANDA	ANDA071611	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	1 TABLET, FILM COATED in 1 BOTTLE (76420-271-01)
76420-271-02	76420-271	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20220903	N/A	ANDA	ANDA071611	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	2 TABLET, FILM COATED in 1 BOTTLE (76420-271-02)