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
76385-101-60	76385-101	HUMAN PRESCRIPTION DRUG	METHSCOPOLAMINE BROMIDE	methscopolamine bromide	TABLET	ORAL	20131001	N/A	ANDA	ANDA200602	BAYSHORE PHARMACEUTICALS LLC	METHSCOPOLAMINE BROMIDE	5 mg/1	60 TABLET in 1 BOTTLE (76385-101-60)
43063-740-01	43063-740	HUMAN PRESCRIPTION DRUG	METHSCOPOLAMINE BROMIDE	methscopolamine bromide	TABLET	ORAL	20170201	N/A	ANDA	ANDA200602	PD-Rx Pharmaceuticals, Inc.	METHSCOPOLAMINE BROMIDE	2.5 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (43063-740-01)
43063-741-60	43063-741	HUMAN PRESCRIPTION DRUG	METHSCOPOLAMINE BROMIDE	methscopolamine bromide	TABLET	ORAL	20170201	N/A	ANDA	ANDA200602	PD-Rx Pharmaceuticals, Inc.	METHSCOPOLAMINE BROMIDE	5 mg/1	60 TABLET in 1 BOTTLE, PLASTIC (43063-741-60)
76385-100-01	76385-100	HUMAN PRESCRIPTION DRUG	METHSCOPOLAMINE BROMIDE	methscopolamine bromide	TABLET	ORAL	20131001	N/A	ANDA	ANDA200602	BAYSHORE PHARMACEUTICALS LLC	METHSCOPOLAMINE BROMIDE	2.5 mg/1	100 TABLET in 1 BOTTLE (76385-100-01)