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
80425-0146-2	80425-0146	HUMAN PRESCRIPTION DRUG	Duloxetine HCL DR	Duloxetine HCL	CAPSULE, DELAYED RELEASE	ORAL	20230614	N/A	ANDA	ANDA208706	Advanced Rx Pharmacy of Tennessee, LLC	DULOXETINE HYDROCHLORIDE	30 mg/1	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0146-2)
80425-0146-3	80425-0146	HUMAN PRESCRIPTION DRUG	Duloxetine HCL DR	Duloxetine HCL	CAPSULE, DELAYED RELEASE	ORAL	20230614	N/A	ANDA	ANDA208706	Advanced Rx Pharmacy of Tennessee, LLC	DULOXETINE HYDROCHLORIDE	30 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0146-3)
80425-0311-1	80425-0311	HUMAN PRESCRIPTION DRUG	Duloxetine DR	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20230407	N/A	ANDA	ANDA208706	Advanced Rx Pharmacy of Tennessee, LLC	DULOXETINE HYDROCHLORIDE	20 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0311-1)
80425-0311-2	80425-0311	HUMAN PRESCRIPTION DRUG	Duloxetine DR	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20230407	N/A	ANDA	ANDA208706	Advanced Rx Pharmacy of Tennessee, LLC	DULOXETINE HYDROCHLORIDE	20 mg/1	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0311-2)
80425-0311-3	80425-0311	HUMAN PRESCRIPTION DRUG	Duloxetine DR	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20230407	N/A	ANDA	ANDA208706	Advanced Rx Pharmacy of Tennessee, LLC	DULOXETINE HYDROCHLORIDE	20 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0311-3)
82009-170-10	82009-170	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20250701	N/A	ANDA	ANDA208706	Quallent Pharmaceuticals Health LLC	DULOXETINE HYDROCHLORIDE	20 mg/1	1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (82009-170-10)
82009-171-10	82009-171	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20250701	N/A	ANDA	ANDA208706	Quallent Pharmaceuticals Health LLC	DULOXETINE HYDROCHLORIDE	30 mg/1	1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (82009-171-10)
82009-172-30	82009-172	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20250701	N/A	ANDA	ANDA208706	Quallent Pharmaceuticals Health LLC	DULOXETINE HYDROCHLORIDE	40 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (82009-172-30)
82009-173-10	82009-173	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20250701	N/A	ANDA	ANDA208706	Quallent Pharmaceuticals Health LLC	DULOXETINE HYDROCHLORIDE	60 mg/1	1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (82009-173-10)