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
70710-1537-3	70710-1537	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20140527	N/A	ANDA	ANDA090728	Zydus Pharmaceuticals USA Inc.	DULOXETINE HYDROCHLORIDE	20 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70710-1537-3)
70710-1538-0	70710-1538	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20170406	N/A	ANDA	ANDA090728	Zydus Pharmaceuticals USA Inc.	DULOXETINE HYDROCHLORIDE	30 mg/1	1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70710-1538-0)
70710-1538-3	70710-1538	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20140527	N/A	ANDA	ANDA090728	Zydus Pharmaceuticals USA Inc.	DULOXETINE HYDROCHLORIDE	30 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70710-1538-3)
70710-1538-9	70710-1538	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20140527	N/A	ANDA	ANDA090728	Zydus Pharmaceuticals USA Inc.	DULOXETINE HYDROCHLORIDE	30 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70710-1538-9)
70710-1539-0	70710-1539	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20170406	N/A	ANDA	ANDA090728	Zydus Pharmaceuticals USA Inc.	DULOXETINE HYDROCHLORIDE	60 mg/1	1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70710-1539-0)
70710-1539-3	70710-1539	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20140527	N/A	ANDA	ANDA090728	Zydus Pharmaceuticals USA Inc.	DULOXETINE HYDROCHLORIDE	60 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70710-1539-3)
70710-1539-9	70710-1539	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20140527	N/A	ANDA	ANDA090728	Zydus Pharmaceuticals USA Inc.	DULOXETINE HYDROCHLORIDE	60 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70710-1539-9)
70710-1537-0	70710-1537	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20170406	N/A	ANDA	ANDA090728	Zydus Pharmaceuticals USA Inc.	DULOXETINE HYDROCHLORIDE	20 mg/1	1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70710-1537-0)
70710-1537-9	70710-1537	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20140527	N/A	ANDA	ANDA090728	Zydus Pharmaceuticals USA Inc.	DULOXETINE HYDROCHLORIDE	20 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70710-1537-9)
70771-1344-6	70771-1344	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20140527	N/A	ANDA	ANDA090728	Zydus Lifesciences Limited	DULOXETINE HYDROCHLORIDE	20 mg/1	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70771-1344-6)
70771-1344-9	70771-1344	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20140527	N/A	ANDA	ANDA090728	Zydus Lifesciences Limited	DULOXETINE HYDROCHLORIDE	20 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70771-1344-9)
70771-1345-0	70771-1345	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20170406	N/A	ANDA	ANDA090728	Zydus Lifesciences Limited	DULOXETINE HYDROCHLORIDE	30 mg/1	1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70771-1345-0)
70771-1345-3	70771-1345	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20140527	N/A	ANDA	ANDA090728	Zydus Lifesciences Limited	DULOXETINE HYDROCHLORIDE	30 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70771-1345-3)
70771-1345-9	70771-1345	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20140527	N/A	ANDA	ANDA090728	Zydus Lifesciences Limited	DULOXETINE HYDROCHLORIDE	30 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70771-1345-9)
70771-1346-0	70771-1346	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20170406	N/A	ANDA	ANDA090728	Zydus Lifesciences Limited	DULOXETINE HYDROCHLORIDE	60 mg/1	1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70771-1346-0)
70771-1346-3	70771-1346	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20140527	N/A	ANDA	ANDA090728	Zydus Lifesciences Limited	DULOXETINE HYDROCHLORIDE	60 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70771-1346-3)
70771-1346-9	70771-1346	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20140527	N/A	ANDA	ANDA090728	Zydus Lifesciences Limited	DULOXETINE HYDROCHLORIDE	60 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70771-1346-9)
70710-1537-6	70710-1537	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20140527	N/A	ANDA	ANDA090728	Zydus Pharmaceuticals USA Inc.	DULOXETINE HYDROCHLORIDE	20 mg/1	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70710-1537-6)
70771-1344-0	70771-1344	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20170406	N/A	ANDA	ANDA090728	Zydus Lifesciences Limited	DULOXETINE HYDROCHLORIDE	20 mg/1	1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70771-1344-0)
70771-1344-3	70771-1344	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20140527	N/A	ANDA	ANDA090728	Zydus Lifesciences Limited	DULOXETINE HYDROCHLORIDE	20 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70771-1344-3)