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
70518-3601-0	70518-3601	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20221230	N/A	ANDA	ANDA204343	REMEDYREPACK INC.	DULOXETINE HYDROCHLORIDE	20 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (70518-3601-0)
68071-2709-3	68071-2709	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20220519	N/A	ANDA	ANDA204343	NuCare Pharmaceuticals,Inc.	DULOXETINE HYDROCHLORIDE	60 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68071-2709-3)
50090-4708-0	50090-4708	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20191111	N/A	ANDA	ANDA204343	A-S Medication Solutions	DULOXETINE HYDROCHLORIDE	20 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-4708-0)
31722-168-01	31722-168	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20201230	N/A	ANDA	ANDA204343	Camber Pharmaceuticals, Inc.	DULOXETINE HYDROCHLORIDE	20 mg/1	100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (31722-168-01)
31722-168-32	31722-168	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20201230	N/A	ANDA	ANDA204343	Camber Pharmaceuticals, Inc.	DULOXETINE HYDROCHLORIDE	20 mg/1	105 CAPSULE, DELAYED RELEASE in 1 CARTON (31722-168-32)
31722-168-60	31722-168	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20201230	N/A	ANDA	ANDA204343	Camber Pharmaceuticals, Inc.	DULOXETINE HYDROCHLORIDE	20 mg/1	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (31722-168-60)
31722-169-01	31722-169	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20201230	N/A	ANDA	ANDA204343	Camber Pharmaceuticals, Inc.	DULOXETINE HYDROCHLORIDE	30 mg/1	100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (31722-169-01)
31722-169-10	31722-169	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20201230	N/A	ANDA	ANDA204343	Camber Pharmaceuticals, Inc.	DULOXETINE HYDROCHLORIDE	30 mg/1	1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (31722-169-10)
31722-169-30	31722-169	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20201230	N/A	ANDA	ANDA204343	Camber Pharmaceuticals, Inc.	DULOXETINE HYDROCHLORIDE	30 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (31722-169-30)
31722-169-31	31722-169	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20201230	N/A	ANDA	ANDA204343	Camber Pharmaceuticals, Inc.	DULOXETINE HYDROCHLORIDE	30 mg/1	7 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (31722-169-31)
31722-169-32	31722-169	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20201230	N/A	ANDA	ANDA204343	Camber Pharmaceuticals, Inc.	DULOXETINE HYDROCHLORIDE	30 mg/1	105 CAPSULE, DELAYED RELEASE in 1 CARTON (31722-169-32)
31722-169-60	31722-169	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20201230	N/A	ANDA	ANDA204343	Camber Pharmaceuticals, Inc.	DULOXETINE HYDROCHLORIDE	30 mg/1	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (31722-169-60)
31722-170-01	31722-170	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20201230	N/A	ANDA	ANDA204343	Camber Pharmaceuticals, Inc.	DULOXETINE HYDROCHLORIDE	60 mg/1	100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (31722-170-01)
31722-170-10	31722-170	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20201230	N/A	ANDA	ANDA204343	Camber Pharmaceuticals, Inc.	DULOXETINE HYDROCHLORIDE	60 mg/1	1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (31722-170-10)
31722-170-30	31722-170	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20201230	N/A	ANDA	ANDA204343	Camber Pharmaceuticals, Inc.	DULOXETINE HYDROCHLORIDE	60 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (31722-170-30)
31722-170-31	31722-170	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20201230	N/A	ANDA	ANDA204343	Camber Pharmaceuticals, Inc.	DULOXETINE HYDROCHLORIDE	60 mg/1	7 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (31722-170-31)
31722-170-32	31722-170	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20201230	N/A	ANDA	ANDA204343	Camber Pharmaceuticals, Inc.	DULOXETINE HYDROCHLORIDE	60 mg/1	105 CAPSULE, DELAYED RELEASE in 1 CARTON (31722-170-32)
31722-170-60	31722-170	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20201230	N/A	ANDA	ANDA204343	Camber Pharmaceuticals, Inc.	DULOXETINE HYDROCHLORIDE	60 mg/1	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (31722-170-60)
31722-168-10	31722-168	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20201230	N/A	ANDA	ANDA204343	Camber Pharmaceuticals, Inc.	DULOXETINE HYDROCHLORIDE	20 mg/1	1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (31722-168-10)
31722-168-30	31722-168	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20201230	N/A	ANDA	ANDA204343	Camber Pharmaceuticals, Inc.	DULOXETINE HYDROCHLORIDE	20 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (31722-168-30)