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
60505-6250-1	60505-6250	HUMAN PRESCRIPTION DRUG	Dexamethasone	Dexamethasone	TABLET	ORAL	20231205	N/A	ANDA	ANDA217695	Apotex Corp.	DEXAMETHASONE	.75 mg/1	100 TABLET in 1 BOTTLE (60505-6250-1)
60505-6254-1	60505-6254	HUMAN PRESCRIPTION DRUG	Dexamethasone	Dexamethasone	TABLET	ORAL	20231101	N/A	ANDA	ANDA217695	Apotex Corp.	DEXAMETHASONE	4 mg/1	100 TABLET in 1 BOTTLE (60505-6254-1)
60505-6249-1	60505-6249	HUMAN PRESCRIPTION DRUG	Dexamethasone	Dexamethasone	TABLET	ORAL	20231205	N/A	ANDA	ANDA217695	Apotex Corp.	DEXAMETHASONE	.5 mg/1	100 TABLET in 1 BOTTLE (60505-6249-1)
60505-6253-1	60505-6253	HUMAN PRESCRIPTION DRUG	Dexamethasone	Dexamethasone	TABLET	ORAL	20231101	N/A	ANDA	ANDA217695	Apotex Corp.	DEXAMETHASONE	2 mg/1	100 TABLET in 1 BOTTLE (60505-6253-1)
60505-6251-1	60505-6251	HUMAN PRESCRIPTION DRUG	Dexamethasone	Dexamethasone	TABLET	ORAL	20231101	N/A	ANDA	ANDA217695	Apotex Corp.	DEXAMETHASONE	1 mg/1	100 TABLET in 1 BOTTLE (60505-6251-1)
60505-6255-1	60505-6255	HUMAN PRESCRIPTION DRUG	Dexamethasone	Dexamethasone	TABLET	ORAL	20231205	N/A	ANDA	ANDA217695	Apotex Corp.	DEXAMETHASONE	6 mg/1	100 TABLET in 1 BOTTLE (60505-6255-1)
82804-157-04	82804-157	HUMAN PRESCRIPTION DRUG	Dexamethasone	Dexamethasone	TABLET	ORAL	20241009	N/A	ANDA	ANDA217695	Proficient Rx LP	DEXAMETHASONE	4 mg/1	4 TABLET in 1 BOTTLE (82804-157-04)
60505-6252-1	60505-6252	HUMAN PRESCRIPTION DRUG	Dexamethasone	Dexamethasone	TABLET	ORAL	20231205	N/A	ANDA	ANDA217695	Apotex Corp.	DEXAMETHASONE	1.5 mg/1	100 TABLET in 1 BOTTLE (60505-6252-1)