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
69306-075-09	69306-075	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20210115	N/A	ANDA	ANDA078722	Doc Rx	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (69306-075-09)
68788-9967-3	68788-9967	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20150501	N/A	ANDA	ANDA078722	Preferred Pharmaceuticals, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68788-9967-3)
68788-9967-7	68788-9967	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20190814	N/A	ANDA	ANDA078722	Preferred Pharmaceuticals, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	8 TABLET, FILM COATED in 1 BOTTLE (68788-9967-7)
68788-9967-8	68788-9967	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20150501	N/A	ANDA	ANDA078722	Preferred Pharmaceuticals, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (68788-9967-8)
68788-9967-9	68788-9967	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20150501	N/A	ANDA	ANDA078722	Preferred Pharmaceuticals, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68788-9967-9)
76420-019-30	76420-019	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20200604	N/A	ANDA	ANDA078722	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (76420-019-30)
76420-019-60	76420-019	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20200604	N/A	ANDA	ANDA078722	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (76420-019-60)
76420-019-90	76420-019	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20200604	N/A	ANDA	ANDA078722	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (76420-019-90)
76420-010-01	76420-010	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20221021	N/A	ANDA	ANDA078722	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (76420-010-01)
76420-010-05	76420-010	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20221021	N/A	ANDA	ANDA078722	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (76420-010-05)
76420-010-12	76420-010	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20230316	N/A	ANDA	ANDA078722	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (76420-010-12)
76420-010-15	76420-010	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20221021	N/A	ANDA	ANDA078722	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (76420-010-15)
76420-010-30	76420-010	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20200123	N/A	ANDA	ANDA078722	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (76420-010-30)
76420-010-60	76420-010	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20200123	N/A	ANDA	ANDA078722	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (76420-010-60)
76420-010-90	76420-010	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20221021	N/A	ANDA	ANDA078722	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (76420-010-90)
68788-9967-2	68788-9967	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20150501	N/A	ANDA	ANDA078722	Preferred Pharmaceuticals, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (68788-9967-2)
68788-9967-1	68788-9967	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20150501	N/A	ANDA	ANDA078722	Preferred Pharmaceuticals, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68788-9967-1)
68788-9967-6	68788-9967	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20150501	N/A	ANDA	ANDA078722	Preferred Pharmaceuticals, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (68788-9967-6)
50090-1848-0	50090-1848	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20150528	N/A	ANDA	ANDA078722	A-S Medication Solutions	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (50090-1848-0)
50090-1848-1	50090-1848	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20150528	N/A	ANDA	ANDA078722	A-S Medication Solutions	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (50090-1848-1)