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
63629-4284-3	63629-4284	HUMAN PRESCRIPTION DRUG	Hydromorphone Hydrochloride	Hydromorphone Hydrochloride	TABLET	ORAL	20101022	N/A	NDA AUTHORIZED GENERIC	NDA019892	Bryant Ranch Prepack	HYDROMORPHONE HYDROCHLORIDE	2 mg/1	30 TABLET in 1 BOTTLE (63629-4284-3)
63629-4284-4	63629-4284	HUMAN PRESCRIPTION DRUG	Hydromorphone Hydrochloride	Hydromorphone Hydrochloride	TABLET	ORAL	20101112	N/A	NDA AUTHORIZED GENERIC	NDA019892	Bryant Ranch Prepack	HYDROMORPHONE HYDROCHLORIDE	2 mg/1	28 TABLET in 1 BOTTLE (63629-4284-4)
63629-4284-5	63629-4284	HUMAN PRESCRIPTION DRUG	Hydromorphone Hydrochloride	Hydromorphone Hydrochloride	TABLET	ORAL	20140611	N/A	NDA AUTHORIZED GENERIC	NDA019892	Bryant Ranch Prepack	HYDROMORPHONE HYDROCHLORIDE	2 mg/1	90 TABLET in 1 BOTTLE (63629-4284-5)
63629-4284-6	63629-4284	HUMAN PRESCRIPTION DRUG	Hydromorphone Hydrochloride	Hydromorphone Hydrochloride	TABLET	ORAL	20120625	N/A	NDA AUTHORIZED GENERIC	NDA019892	Bryant Ranch Prepack	HYDROMORPHONE HYDROCHLORIDE	2 mg/1	120 TABLET in 1 BOTTLE (63629-4284-6)
63629-4284-7	63629-4284	HUMAN PRESCRIPTION DRUG	Hydromorphone Hydrochloride	Hydromorphone Hydrochloride	TABLET	ORAL	20140127	N/A	NDA AUTHORIZED GENERIC	NDA019892	Bryant Ranch Prepack	HYDROMORPHONE HYDROCHLORIDE	2 mg/1	40 TABLET in 1 BOTTLE (63629-4284-7)
63629-4284-8	63629-4284	HUMAN PRESCRIPTION DRUG	Hydromorphone Hydrochloride	Hydromorphone Hydrochloride	TABLET	ORAL	20120501	N/A	NDA AUTHORIZED GENERIC	NDA019892	Bryant Ranch Prepack	HYDROMORPHONE HYDROCHLORIDE	2 mg/1	20 TABLET in 1 BOTTLE (63629-4284-8)
63629-4284-9	63629-4284	HUMAN PRESCRIPTION DRUG	Hydromorphone Hydrochloride	Hydromorphone Hydrochloride	TABLET	ORAL	20200824	N/A	NDA AUTHORIZED GENERIC	NDA019892	Bryant Ranch Prepack	HYDROMORPHONE HYDROCHLORIDE	2 mg/1	10 TABLET in 1 BOTTLE (63629-4284-9)