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
59651-279-99	59651-279	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine Hydrochloride	CAPSULE, DELAYED RELEASE	ORAL	20131211	N/A	ANDA	ANDA090778	Aurobindo Pharma Limited	DULOXETINE HYDROCHLORIDE	20 mg/1	1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (59651-279-99)
59651-280-99	59651-280	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine Hydrochloride	CAPSULE, DELAYED RELEASE	ORAL	20131211	N/A	ANDA	ANDA090778	Aurobindo Pharma Limited	DULOXETINE HYDROCHLORIDE	30 mg/1	1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (59651-280-99)
63187-612-30	63187-612	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine Hydrochloride	CAPSULE, DELAYED RELEASE	ORAL	20181201	N/A	ANDA	ANDA090778	Proficient Rx LP	DULOXETINE HYDROCHLORIDE	30 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (63187-612-30)
63187-612-60	63187-612	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine Hydrochloride	CAPSULE, DELAYED RELEASE	ORAL	20181201	N/A	ANDA	ANDA090778	Proficient Rx LP	DULOXETINE HYDROCHLORIDE	30 mg/1	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (63187-612-60)
0904-7043-04	0904-7043	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine Hydrochloride	CAPSULE, DELAYED RELEASE	ORAL	20131211	20260331	ANDA	ANDA090778	Major Pharmaceuticals	DULOXETINE HYDROCHLORIDE	20 mg/1	30 BLISTER PACK in 1 CARTON (0904-7043-04) / 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK
0904-7043-61	0904-7043	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine Hydrochloride	CAPSULE, DELAYED RELEASE	ORAL	20131211	20251231	ANDA	ANDA090778	Major Pharmaceuticals	DULOXETINE HYDROCHLORIDE	20 mg/1	100 BLISTER PACK in 1 CARTON (0904-7043-61) / 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK
63187-612-90	63187-612	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine Hydrochloride	CAPSULE, DELAYED RELEASE	ORAL	20181201	N/A	ANDA	ANDA090778	Proficient Rx LP	DULOXETINE HYDROCHLORIDE	30 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (63187-612-90)