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
50090-6281-0	50090-6281	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20221215	N/A	ANDA	ANDA090694	A-S Medication Solutions	DULOXETINE HYDROCHLORIDE	30 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-6281-0)
50090-6281-1	50090-6281	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20221215	N/A	ANDA	ANDA090694	A-S Medication Solutions	DULOXETINE HYDROCHLORIDE	30 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-6281-1)
50090-6406-0	50090-6406	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20230323	N/A	ANDA	ANDA090694	A-S Medication Solutions	DULOXETINE HYDROCHLORIDE	20 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-6406-0)
50090-6406-1	50090-6406	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20230724	N/A	ANDA	ANDA090694	A-S Medication Solutions	DULOXETINE HYDROCHLORIDE	20 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-6406-1)
50090-6775-0	50090-6775	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20231024	N/A	ANDA	ANDA090694	A-S Medication Solutions	DULOXETINE HYDROCHLORIDE	60 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-6775-0)
70518-1765-1	70518-1765	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20250122	N/A	ANDA	ANDA090694	REMEDYREPACK INC.	DULOXETINE HYDROCHLORIDE	30 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-1765-1)
70518-1765-2	70518-1765	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20250623	N/A	ANDA	ANDA090694	REMEDYREPACK INC.	DULOXETINE HYDROCHLORIDE	30 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-1765-2)
70518-1765-3	70518-1765	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20250808	N/A	ANDA	ANDA090694	REMEDYREPACK INC.	DULOXETINE HYDROCHLORIDE	30 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (70518-1765-3)
83008-040-30	83008-040	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20230911	20260131	ANDA	ANDA090694	Quality Care Products, LLC	DULOXETINE HYDROCHLORIDE	60 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (83008-040-30)
83008-040-60	83008-040	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20230911	20251231	ANDA	ANDA090694	Quality Care Products, LLC	DULOXETINE HYDROCHLORIDE	60 mg/1	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (83008-040-60)
83008-046-30	83008-046	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20240215	20260228	ANDA	ANDA090694	Quality Care Products, LLC	DULOXETINE HYDROCHLORIDE	30 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (83008-046-30)
50090-6775-1	50090-6775	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20231024	N/A	ANDA	ANDA090694	A-S Medication Solutions	DULOXETINE HYDROCHLORIDE	60 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-6775-1)
70518-1244-1	70518-1244	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20250324	N/A	ANDA	ANDA090694	REMEDYREPACK INC.	DULOXETINE HYDROCHLORIDE	60 mg/1	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-1244-1)
70518-1244-2	70518-1244	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20250416	N/A	ANDA	ANDA090694	REMEDYREPACK INC.	DULOXETINE HYDROCHLORIDE	60 mg/1	180 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-1244-2)