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
72162-1485-1	72162-1485	HUMAN PRESCRIPTION DRUG	Doxylamine Succinate and Pyridoxine Hydrochloride	Doxylamine Succinate and Pyridoxine Hydrochloride, Delayed release Tablets 10 mg/10 mg	TABLET, DELAYED RELEASE	ORAL	20230830	N/A	ANDA	ANDA208518	Bryant Ranch Prepack	DOXYLAMINE SUCCINATE; PYRIDOXINE HYDROCHLORIDE	10 mg/1; 10 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-1485-1)
63629-2184-1	63629-2184	HUMAN PRESCRIPTION DRUG	Doxylamine Succinate and Pyridoxine Hydrochloride	Doxylamine Succinate and Pyridoxine Hydrochloride, Delayed release Tablets 10 mg/10 mg	TABLET, DELAYED RELEASE	ORAL	20210312	N/A	ANDA	ANDA208518	Bryant Ranch Prepack	DOXYLAMINE SUCCINATE; PYRIDOXINE HYDROCHLORIDE	10 mg/1; 10 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE (63629-2184-1)
49884-186-01	49884-186	HUMAN PRESCRIPTION DRUG	Doxylamine Succinate and Pyridoxine Hydrochloride	Doxylamine Succinate and Pyridoxine Hydrochloride, Delayed release Tablets 10 mg/10 mg	TABLET, DELAYED RELEASE	ORAL	20191219	N/A	ANDA	ANDA208518	Par Pharmaceutical, Inc.	DOXYLAMINE SUCCINATE; PYRIDOXINE HYDROCHLORIDE	10 mg/1; 10 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE (49884-186-01)