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
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)
60687-745-01	60687-745	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine Hydrochloride	CAPSULE, DELAYED RELEASE	ORAL	20230420	20260531	ANDA	ANDA090778	American Health Packaging	DULOXETINE HYDROCHLORIDE	60 mg/1	100 BLISTER PACK in 1 CARTON (60687-745-01) / 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (60687-745-11)
59651-279-60	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	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (59651-279-60)
59651-279-78	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	10 BLISTER PACK in 1 CARTON (59651-279-78) / 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (59651-279-10)
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)
59651-280-30	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)
59651-282-30	59651-282	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine Hydrochloride	CAPSULE, DELAYED RELEASE	ORAL	20131211	N/A	ANDA	ANDA090778	Aurobindo Pharma Limited	DULOXETINE HYDROCHLORIDE	60 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (59651-282-30)
59651-282-78	59651-282	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine Hydrochloride	CAPSULE, DELAYED RELEASE	ORAL	20131211	N/A	ANDA	ANDA090778	Aurobindo Pharma Limited	DULOXETINE HYDROCHLORIDE	60 mg/1	10 BLISTER PACK in 1 CARTON (59651-282-78) / 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (59651-282-10)
59651-282-90	59651-282	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine Hydrochloride	CAPSULE, DELAYED RELEASE	ORAL	20131211	N/A	ANDA	ANDA090778	Aurobindo Pharma Limited	DULOXETINE HYDROCHLORIDE	60 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (59651-282-90)
59651-282-99	59651-282	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine Hydrochloride	CAPSULE, DELAYED RELEASE	ORAL	20131211	N/A	ANDA	ANDA090778	Aurobindo Pharma Limited	DULOXETINE HYDROCHLORIDE	60 mg/1	1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (59651-282-99)
60760-951-60	60760-951	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine Hydrochloride	CAPSULE, DELAYED RELEASE	ORAL	20230724	N/A	ANDA	ANDA090778	ST. MARY'S MEDICAL PARK PHARMACY	DULOXETINE HYDROCHLORIDE	30 mg/1	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-951-60)
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)
43063-878-30	43063-878	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine Hydrochloride	CAPSULE, DELAYED RELEASE	ORAL	20180806	N/A	ANDA	ANDA090778	PD-Rx Pharmaceuticals, Inc.	DULOXETINE HYDROCHLORIDE	60 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (43063-878-30)
43063-878-90	43063-878	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine Hydrochloride	CAPSULE, DELAYED RELEASE	ORAL	20200727	N/A	ANDA	ANDA090778	PD-Rx Pharmaceuticals, Inc.	DULOXETINE HYDROCHLORIDE	60 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (43063-878-90)