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
13811-704-10	13811-704	HUMAN PRESCRIPTION DRUG	Hydromorphone Hydrochloride	Hydromorphone Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20160915	N/A	ANDA	ANDA205629	Trigen Laboratories, LLC	HYDROMORPHONE HYDROCHLORIDE	32 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (13811-704-10)
13811-702-10	13811-702	HUMAN PRESCRIPTION DRUG	Hydromorphone Hydrochloride	Hydromorphone Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20160915	N/A	ANDA	ANDA205629	Trigen Laboratories, LLC	HYDROMORPHONE HYDROCHLORIDE	12 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (13811-702-10)
13811-701-10	13811-701	HUMAN PRESCRIPTION DRUG	Hydromorphone Hydrochloride	Hydromorphone Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20160915	N/A	ANDA	ANDA205629	Trigen Laboratories, LLC	HYDROMORPHONE HYDROCHLORIDE	8 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (13811-701-10)
13811-703-10	13811-703	HUMAN PRESCRIPTION DRUG	Hydromorphone Hydrochloride	Hydromorphone Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20160915	N/A	ANDA	ANDA205629	Trigen Laboratories, LLC	HYDROMORPHONE HYDROCHLORIDE	16 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (13811-703-10)