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
0574-0297-01	0574-0297	HUMAN PRESCRIPTION DRUG	hydromorphone hydrochloride	hydromorphone hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20170929	N/A	ANDA	ANDA204278	Padagis US LLC	HYDROMORPHONE HYDROCHLORIDE	32 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0574-0297-01)
0574-0295-01	0574-0295	HUMAN PRESCRIPTION DRUG	hydromorphone hydrochloride	hydromorphone hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20150522	N/A	ANDA	ANDA204278	Padagis US LLC	HYDROMORPHONE HYDROCHLORIDE	16 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0574-0295-01)
0574-0294-01	0574-0294	HUMAN PRESCRIPTION DRUG	hydromorphone hydrochloride	hydromorphone hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20150522	N/A	ANDA	ANDA204278	Padagis US LLC	HYDROMORPHONE HYDROCHLORIDE	12 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0574-0294-01)
0574-0293-01	0574-0293	HUMAN PRESCRIPTION DRUG	hydromorphone hydrochloride	hydromorphone hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20150522	N/A	ANDA	ANDA204278	Padagis US LLC	HYDROMORPHONE HYDROCHLORIDE	8 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0574-0293-01)