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
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)
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)
70518-0937-7	70518-0937	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine Hydrochloride	CAPSULE, DELAYED RELEASE	ORAL	20240415	N/A	ANDA	ANDA090778	REMEDYREPACK INC.	DULOXETINE HYDROCHLORIDE	60 mg/1	180 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-0937-7)
70518-0937-5	70518-0937	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine Hydrochloride	CAPSULE, DELAYED RELEASE	ORAL	20221128	N/A	ANDA	ANDA090778	REMEDYREPACK INC.	DULOXETINE HYDROCHLORIDE	60 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-0937-5)
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)
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)
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)
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)
71610-401-83	71610-401	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine Hydrochloride	CAPSULE, DELAYED RELEASE	ORAL	20200226	N/A	ANDA	ANDA090778	Aphena Pharma Solutions - Tennessee, LLC	DULOXETINE HYDROCHLORIDE	20 mg/1	3600 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71610-401-83)
71610-402-60	71610-402	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine Hydrochloride	CAPSULE, DELAYED RELEASE	ORAL	20200226	N/A	ANDA	ANDA090778	Aphena Pharma Solutions - Tennessee, LLC	DULOXETINE HYDROCHLORIDE	30 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71610-402-60)
57237-019-30	57237-019	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine Hydrochloride	CAPSULE, DELAYED RELEASE	ORAL	20131211	N/A	ANDA	ANDA090778	Rising Pharma Holdings, Inc.	DULOXETINE HYDROCHLORIDE	60 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (57237-019-30)
57237-019-90	57237-019	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine Hydrochloride	CAPSULE, DELAYED RELEASE	ORAL	20131211	N/A	ANDA	ANDA090778	Rising Pharma Holdings, Inc.	DULOXETINE HYDROCHLORIDE	60 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (57237-019-90)
57237-019-99	57237-019	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine Hydrochloride	CAPSULE, DELAYED RELEASE	ORAL	20131211	N/A	ANDA	ANDA090778	Rising Pharma Holdings, Inc.	DULOXETINE HYDROCHLORIDE	60 mg/1	1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (57237-019-99)