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
31722-122-01	31722-122	HUMAN PRESCRIPTION DRUG	hydromorphone hydrochloride	hydromorphone hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20200924	N/A	ANDA	ANDA212133	Camber Pharmaceuticals, Inc.	HYDROMORPHONE HYDROCHLORIDE	32 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-122-01)
72865-170-01	72865-170	HUMAN PRESCRIPTION DRUG	hydromorphone hydrochloride	hydromorphone hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20200924	N/A	ANDA	ANDA212133	XLCare Pharmaceuticals, Inc.	HYDROMORPHONE HYDROCHLORIDE	16 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72865-170-01)
31722-119-01	31722-119	HUMAN PRESCRIPTION DRUG	hydromorphone hydrochloride	hydromorphone hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20200924	N/A	ANDA	ANDA212133	Camber Pharmaceuticals, Inc.	HYDROMORPHONE HYDROCHLORIDE	8 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-119-01)
72865-171-01	72865-171	HUMAN PRESCRIPTION DRUG	hydromorphone hydrochloride	hydromorphone hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20200924	N/A	ANDA	ANDA212133	XLCare Pharmaceuticals, Inc.	HYDROMORPHONE HYDROCHLORIDE	32 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72865-171-01)
31722-121-01	31722-121	HUMAN PRESCRIPTION DRUG	hydromorphone hydrochloride	hydromorphone hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20200924	N/A	ANDA	ANDA212133	Camber Pharmaceuticals, Inc.	HYDROMORPHONE HYDROCHLORIDE	16 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-121-01)
72865-169-01	72865-169	HUMAN PRESCRIPTION DRUG	hydromorphone hydrochloride	hydromorphone hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20200924	N/A	ANDA	ANDA212133	XLCare Pharmaceuticals, Inc.	HYDROMORPHONE HYDROCHLORIDE	12 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72865-169-01)
31722-120-01	31722-120	HUMAN PRESCRIPTION DRUG	hydromorphone hydrochloride	hydromorphone hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20200924	N/A	ANDA	ANDA212133	Camber Pharmaceuticals, Inc.	HYDROMORPHONE HYDROCHLORIDE	12 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-120-01)
72865-168-01	72865-168	HUMAN PRESCRIPTION DRUG	hydromorphone hydrochloride	hydromorphone hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20200924	N/A	ANDA	ANDA212133	XLCare Pharmaceuticals, Inc.	HYDROMORPHONE HYDROCHLORIDE	8 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72865-168-01)