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
72189-283-15	72189-283	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	CYCLOBENZAPRINE HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20211019	N/A	ANDA	ANDA208170	DirectRx	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (72189-283-15)
72189-283-20	72189-283	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	CYCLOBENZAPRINE HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20211019	N/A	ANDA	ANDA208170	DirectRx	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (72189-283-20)
72189-283-30	72189-283	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	CYCLOBENZAPRINE HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20211019	N/A	ANDA	ANDA208170	DirectRx	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (72189-283-30)
72189-283-60	72189-283	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	CYCLOBENZAPRINE HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20211019	N/A	ANDA	ANDA208170	DirectRx	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (72189-283-60)
72189-283-82	72189-283	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	CYCLOBENZAPRINE HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20211019	N/A	ANDA	ANDA208170	DirectRx	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (72189-283-82)
72189-283-90	72189-283	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	CYCLOBENZAPRINE HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20211019	N/A	ANDA	ANDA208170	DirectRx	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (72189-283-90)
76420-011-01	76420-011	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20200123	N/A	ANDA	ANDA208170	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	1 TABLET, FILM COATED in 1 BOTTLE (76420-011-01)
76420-011-02	76420-011	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20200123	N/A	ANDA	ANDA208170	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	2 TABLET, FILM COATED in 1 BOTTLE (76420-011-02)
76420-011-04	76420-011	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20250411	N/A	ANDA	ANDA208170	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	4 TABLET, FILM COATED in 1 BOTTLE (76420-011-04)
76420-011-05	76420-011	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20241224	N/A	ANDA	ANDA208170	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	5 TABLET, FILM COATED in 1 BOTTLE (76420-011-05)
76420-011-07	76420-011	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20200123	N/A	ANDA	ANDA208170	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	7 TABLET, FILM COATED in 1 BOTTLE (76420-011-07)
76420-011-12	76420-011	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20250411	N/A	ANDA	ANDA208170	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (76420-011-12)
76420-011-20	76420-011	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20200123	N/A	ANDA	ANDA208170	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (76420-011-20)
76420-011-30	76420-011	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20200123	N/A	ANDA	ANDA208170	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (76420-011-30)
76420-011-60	76420-011	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20200123	N/A	ANDA	ANDA208170	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (76420-011-60)
76420-011-90	76420-011	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20220810	N/A	ANDA	ANDA208170	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (76420-011-90)
76420-030-01	76420-030	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20200619	N/A	ANDA	ANDA208170	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (76420-030-01)
76420-030-05	76420-030	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20200619	N/A	ANDA	ANDA208170	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (76420-030-05)
76420-030-12	76420-030	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20220729	N/A	ANDA	ANDA208170	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (76420-030-12)
76420-030-30	76420-030	HUMAN PRESCRIPTION DRUG	CYCLOBENZAPRINE HYDROCHLORIDE	cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20200619	N/A	ANDA	ANDA208170	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (76420-030-30)