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
76385-130-01	76385-130	HUMAN PRESCRIPTION DRUG	Cyproheptadine Hydrochloride	Cyproheptadine Hydrochloride	TABLET	ORAL	20200301	N/A	ANDA	ANDA206676	Bayshore Pharmaceuticals LLC	CYPROHEPTADINE HYDROCHLORIDE	4 mg/1	100 TABLET in 1 BOTTLE (76385-130-01)
76385-130-10	76385-130	HUMAN PRESCRIPTION DRUG	Cyproheptadine Hydrochloride	Cyproheptadine Hydrochloride	TABLET	ORAL	20200301	N/A	ANDA	ANDA206676	Bayshore Pharmaceuticals LLC	CYPROHEPTADINE HYDROCHLORIDE	4 mg/1	1000 TABLET in 1 BOTTLE (76385-130-10)
72789-102-01	72789-102	HUMAN PRESCRIPTION DRUG	Cyproheptadine Hydrochloride	Cyproheptadine Hydrochloride	TABLET	ORAL	20230710	N/A	ANDA	ANDA206676	PD-Rx Pharmaceuticals, Inc.	CYPROHEPTADINE HYDROCHLORIDE	4 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (72789-102-01)
72789-102-30	72789-102	HUMAN PRESCRIPTION DRUG	Cyproheptadine Hydrochloride	Cyproheptadine Hydrochloride	TABLET	ORAL	20200727	N/A	ANDA	ANDA206676	PD-Rx Pharmaceuticals, Inc.	CYPROHEPTADINE HYDROCHLORIDE	4 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (72789-102-30)