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
50090-6129-1	50090-6129	HUMAN PRESCRIPTION DRUG	CYPROHEPTADINE HYDROCHLORIDE	CYPROHEPTADINE HYDROCHLORIDE	TABLET	ORAL	20221003	N/A	ANDA	ANDA208938	A-S Medication Solutions	CYPROHEPTADINE HYDROCHLORIDE	4 mg/1	30 TABLET in 1 BOTTLE (50090-6129-1)
70771-1076-0	70771-1076	HUMAN PRESCRIPTION DRUG	CYPROHEPTADINE HYDROCHLORIDE	CYPROHEPTADINE HYDROCHLORIDE	TABLET	ORAL	20170720	N/A	ANDA	ANDA208938	Zydus Lifesciences Limited	CYPROHEPTADINE HYDROCHLORIDE	4 mg/1	1000 TABLET in 1 BOTTLE (70771-1076-0)
70771-1076-1	70771-1076	HUMAN PRESCRIPTION DRUG	CYPROHEPTADINE HYDROCHLORIDE	CYPROHEPTADINE HYDROCHLORIDE	TABLET	ORAL	20170720	N/A	ANDA	ANDA208938	Zydus Lifesciences Limited	CYPROHEPTADINE HYDROCHLORIDE	4 mg/1	100 TABLET in 1 BOTTLE (70771-1076-1)
70710-1110-0	70710-1110	HUMAN PRESCRIPTION DRUG	CYPROHEPTADINE HYDROCHLORIDE	CYPROHEPTADINE HYDROCHLORIDE	TABLET	ORAL	20170720	N/A	ANDA	ANDA208938	Zydus Pharmaceuticals USA Inc.	CYPROHEPTADINE HYDROCHLORIDE	4 mg/1	1000 TABLET in 1 BOTTLE (70710-1110-0)
70710-1110-1	70710-1110	HUMAN PRESCRIPTION DRUG	CYPROHEPTADINE HYDROCHLORIDE	CYPROHEPTADINE HYDROCHLORIDE	TABLET	ORAL	20170720	N/A	ANDA	ANDA208938	Zydus Pharmaceuticals USA Inc.	CYPROHEPTADINE HYDROCHLORIDE	4 mg/1	100 TABLET in 1 BOTTLE (70710-1110-1)