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
42708-177-21	42708-177	HUMAN PRESCRIPTION DRUG	Cyproheptadine Hydrochloride	Cyproheptadine Hydrochloride	TABLET	ORAL	20230605	N/A	ANDA	ANDA206553	QPharma Inc	CYPROHEPTADINE HYDROCHLORIDE	4 mg/1	21 TABLET in 1 BOTTLE, PLASTIC (42708-177-21)
50090-5491-1	50090-5491	HUMAN PRESCRIPTION DRUG	Cyproheptadine Hydrochloride	Cyproheptadine Hydrochloride	TABLET	ORAL	20210316	N/A	ANDA	ANDA206553	A-S Medication Solutions	CYPROHEPTADINE HYDROCHLORIDE	4 mg/1	30 TABLET in 1 BOTTLE (50090-5491-1)
52817-210-10	52817-210	HUMAN PRESCRIPTION DRUG	Cyproheptadine Hydrochloride	Cyproheptadine Hydrochloride	TABLET	ORAL	20170117	N/A	ANDA	ANDA206553	TRUPHARMA, LLC	CYPROHEPTADINE HYDROCHLORIDE	4 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (52817-210-10)
52817-210-50	52817-210	HUMAN PRESCRIPTION DRUG	Cyproheptadine Hydrochloride	Cyproheptadine Hydrochloride	TABLET	ORAL	20170117	N/A	ANDA	ANDA206553	TRUPHARMA, LLC	CYPROHEPTADINE HYDROCHLORIDE	4 mg/1	500 TABLET in 1 BOTTLE, PLASTIC (52817-210-50)