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
47335-381-83	47335-381	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20131211	N/A	ANDA	ANDA090745	Sun Pharmaceutical Industries, Inc.	DULOXETINE HYDROCHLORIDE	20 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-381-83)
47335-381-86	47335-381	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20131211	N/A	ANDA	ANDA090745	Sun Pharmaceutical Industries, Inc.	DULOXETINE HYDROCHLORIDE	20 mg/1	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-381-86)
47335-381-88	47335-381	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20131211	N/A	ANDA	ANDA090745	Sun Pharmaceutical Industries, Inc.	DULOXETINE HYDROCHLORIDE	20 mg/1	100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-381-88)
47335-382-08	47335-382	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20131211	N/A	ANDA	ANDA090745	Sun Pharmaceutical Industries, Inc.	DULOXETINE HYDROCHLORIDE	30 mg/1	100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-382-08)
47335-382-18	47335-382	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20131211	N/A	ANDA	ANDA090745	Sun Pharmaceutical Industries, Inc.	DULOXETINE HYDROCHLORIDE	30 mg/1	1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-382-18)
47335-382-61	47335-382	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20131211	N/A	ANDA	ANDA090745	Sun Pharmaceutical Industries, Inc.	DULOXETINE HYDROCHLORIDE	30 mg/1	100 BLISTER PACK in 1 CARTON (47335-382-61) / 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK
47335-382-81	47335-382	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20131211	N/A	ANDA	ANDA090745	Sun Pharmaceutical Industries, Inc.	DULOXETINE HYDROCHLORIDE	30 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-382-81)
47335-382-83	47335-382	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20131211	N/A	ANDA	ANDA090745	Sun Pharmaceutical Industries, Inc.	DULOXETINE HYDROCHLORIDE	30 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-382-83)
47335-382-88	47335-382	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20131211	N/A	ANDA	ANDA090745	Sun Pharmaceutical Industries, Inc.	DULOXETINE HYDROCHLORIDE	30 mg/1	100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-382-88)
47335-383-08	47335-383	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20131211	N/A	ANDA	ANDA090745	Sun Pharmaceutical Industries, Inc.	DULOXETINE HYDROCHLORIDE	60 mg/1	100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-383-08)
47335-383-18	47335-383	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20131211	N/A	ANDA	ANDA090745	Sun Pharmaceutical Industries, Inc.	DULOXETINE HYDROCHLORIDE	60 mg/1	1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-383-18)
47335-383-61	47335-383	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20131211	N/A	ANDA	ANDA090745	Sun Pharmaceutical Industries, Inc.	DULOXETINE HYDROCHLORIDE	60 mg/1	100 BLISTER PACK in 1 CARTON (47335-383-61) / 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK
47335-383-83	47335-383	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20131211	N/A	ANDA	ANDA090745	Sun Pharmaceutical Industries, Inc.	DULOXETINE HYDROCHLORIDE	60 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-383-83)
47335-383-88	47335-383	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20131211	N/A	ANDA	ANDA090745	Sun Pharmaceutical Industries, Inc.	DULOXETINE HYDROCHLORIDE	60 mg/1	100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-383-88)
47335-381-61	47335-381	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20131211	N/A	ANDA	ANDA090745	Sun Pharmaceutical Industries, Inc.	DULOXETINE HYDROCHLORIDE	20 mg/1	100 BLISTER PACK in 1 CARTON (47335-381-61) / 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK
47335-381-18	47335-381	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20131211	N/A	ANDA	ANDA090745	Sun Pharmaceutical Industries, Inc.	DULOXETINE HYDROCHLORIDE	20 mg/1	1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-381-18)
47335-381-08	47335-381	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20131211	N/A	ANDA	ANDA090745	Sun Pharmaceutical Industries, Inc.	DULOXETINE HYDROCHLORIDE	20 mg/1	100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-381-08)
61919-483-30	61919-483	HUMAN PRESCRIPTION DRUG	DULOXETINE	DULOXETINE	CAPSULE, DELAYED RELEASE	ORAL	20150101	N/A	ANDA	ANDA090745	DIRECT RX	DULOXETINE HYDROCHLORIDE	60 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (61919-483-30)