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
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)
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)
70518-0937-3	70518-0937	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine Hydrochloride	CAPSULE, DELAYED RELEASE	ORAL	20220906	N/A	ANDA	ANDA090778	REMEDYREPACK INC.	DULOXETINE HYDROCHLORIDE	60 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-0937-3)
70518-0937-4	70518-0937	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine Hydrochloride	CAPSULE, DELAYED RELEASE	ORAL	20220906	N/A	ANDA	ANDA090778	REMEDYREPACK INC.	DULOXETINE HYDROCHLORIDE	60 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (70518-0937-4)
70518-0937-6	70518-0937	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine Hydrochloride	CAPSULE, DELAYED RELEASE	ORAL	20221128	N/A	ANDA	ANDA090778	REMEDYREPACK INC.	DULOXETINE HYDROCHLORIDE	60 mg/1	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-0937-6)
63187-666-30	63187-666	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine Hydrochloride	CAPSULE, DELAYED RELEASE	ORAL	20181201	N/A	ANDA	ANDA090778	Proficient Rx LP	DULOXETINE HYDROCHLORIDE	60 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (63187-666-30)
63187-666-60	63187-666	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine Hydrochloride	CAPSULE, DELAYED RELEASE	ORAL	20181201	N/A	ANDA	ANDA090778	Proficient Rx LP	DULOXETINE HYDROCHLORIDE	60 mg/1	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (63187-666-60)
57237-017-60	57237-017	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine Hydrochloride	CAPSULE, DELAYED RELEASE	ORAL	20131211	N/A	ANDA	ANDA090778	Rising Pharma Holdings, Inc.	DULOXETINE HYDROCHLORIDE	20 mg/1	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (57237-017-60)
57237-017-99	57237-017	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine Hydrochloride	CAPSULE, DELAYED RELEASE	ORAL	20131211	N/A	ANDA	ANDA090778	Rising Pharma Holdings, Inc.	DULOXETINE HYDROCHLORIDE	20 mg/1	1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (57237-017-99)
60687-723-21	60687-723	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine Hydrochloride	CAPSULE, DELAYED RELEASE	ORAL	20230425	20260531	ANDA	ANDA090778	American Health Packaging	DULOXETINE HYDROCHLORIDE	20 mg/1	30 BLISTER PACK in 1 CARTON (60687-723-21) / 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (60687-723-11)
43063-877-90	43063-877	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine Hydrochloride	CAPSULE, DELAYED RELEASE	ORAL	20180806	N/A	ANDA	ANDA090778	PD-Rx Pharmaceuticals, Inc.	DULOXETINE HYDROCHLORIDE	30 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (43063-877-90)
59651-280-30	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	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (59651-280-30)
59651-280-78	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	10 BLISTER PACK in 1 CARTON (59651-280-78) / 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (59651-280-10)
59651-280-90	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	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (59651-280-90)
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)
57237-018-30	57237-018	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine Hydrochloride	CAPSULE, DELAYED RELEASE	ORAL	20131211	N/A	ANDA	ANDA090778	Rising Pharma Holdings, Inc.	DULOXETINE HYDROCHLORIDE	30 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (57237-018-30)
57237-018-90	57237-018	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine Hydrochloride	CAPSULE, DELAYED RELEASE	ORAL	20131211	N/A	ANDA	ANDA090778	Rising Pharma Holdings, Inc.	DULOXETINE HYDROCHLORIDE	30 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (57237-018-90)
57237-018-99	57237-018	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine Hydrochloride	CAPSULE, DELAYED RELEASE	ORAL	20131211	N/A	ANDA	ANDA090778	Rising Pharma Holdings, Inc.	DULOXETINE HYDROCHLORIDE	30 mg/1	1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (57237-018-99)
60687-734-01	60687-734	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine Hydrochloride	CAPSULE, DELAYED RELEASE	ORAL	20230403	20260331	ANDA	ANDA090778	American Health Packaging	DULOXETINE HYDROCHLORIDE	30 mg/1	100 BLISTER PACK in 1 CARTON (60687-734-01) / 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (60687-734-11)