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
0406-3243-01	0406-3243	HUMAN PRESCRIPTION DRUG	Hydromorphone Hydrochloride	hydromorphone hydrochloride	TABLET	ORAL	20041223	N/A	ANDA	ANDA076855	SpecGx LLC	HYDROMORPHONE HYDROCHLORIDE	2 mg/1	100 TABLET in 1 BOTTLE (0406-3243-01)
0406-3244-01	0406-3244	HUMAN PRESCRIPTION DRUG	Hydromorphone Hydrochloride	hydromorphone hydrochloride	TABLET	ORAL	20041223	N/A	ANDA	ANDA076855	SpecGx LLC	HYDROMORPHONE HYDROCHLORIDE	4 mg/1	100 TABLET in 1 BOTTLE (0406-3244-01)
0406-3249-01	0406-3249	HUMAN PRESCRIPTION DRUG	Hydromorphone Hydrochloride	hydromorphone hydrochloride	TABLET	ORAL	20041223	N/A	ANDA	ANDA076855	SpecGx LLC	HYDROMORPHONE HYDROCHLORIDE	8 mg/1	100 TABLET in 1 BOTTLE (0406-3249-01)
60687-579-01	60687-579	HUMAN PRESCRIPTION DRUG	Hydromorphone Hydrochloride	Hydromorphone Hydrochloride	TABLET	ORAL	20210511	N/A	ANDA	ANDA076855	American Health Packaging	HYDROMORPHONE HYDROCHLORIDE	2 mg/1	100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-579-01) / 1 TABLET in 1 BLISTER PACK (60687-579-11)
60687-590-01	60687-590	HUMAN PRESCRIPTION DRUG	Hydromorphone Hydrochloride	hydromorphone hydrochloride	TABLET	ORAL	20210511	N/A	ANDA	ANDA076855	American Health Packaging	HYDROMORPHONE HYDROCHLORIDE	4 mg/1	100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-590-01) / 1 TABLET in 1 BLISTER PACK (60687-590-11)