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
71610-218-30	71610-218	HUMAN PRESCRIPTION DRUG	Duloxetine Delayed-Release	DULOXETINE HYDROCHLORIDE	CAPSULE, DELAYED RELEASE PELLETS	ORAL	20190107	N/A	ANDA	ANDA203088	Aphena Pharma Solutions - Tennessee, LLC	DULOXETINE HYDROCHLORIDE	30 mg/1	30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71610-218-30)
71610-218-60	71610-218	HUMAN PRESCRIPTION DRUG	Duloxetine Delayed-Release	DULOXETINE HYDROCHLORIDE	CAPSULE, DELAYED RELEASE PELLETS	ORAL	20190107	N/A	ANDA	ANDA203088	Aphena Pharma Solutions - Tennessee, LLC	DULOXETINE HYDROCHLORIDE	30 mg/1	90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71610-218-60)
68001-368-04	68001-368	HUMAN PRESCRIPTION DRUG	Duloxetine Delayed-Release	DULOXETINE HYDROCHLORIDE	CAPSULE, DELAYED RELEASE PELLETS	ORAL	20180521	N/A	ANDA	ANDA203088	BluePoint Laboratories	DULOXETINE HYDROCHLORIDE	40 mg/1	30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68001-368-04)
51991-746-05	51991-746	HUMAN PRESCRIPTION DRUG	Duloxetine Delayed-Release	DULOXETINE HYDROCHLORIDE	CAPSULE, DELAYED RELEASE PELLETS	ORAL	20140611	N/A	ANDA	ANDA203088	Breckenridge Pharmaceutical, Inc.	DULOXETINE HYDROCHLORIDE	20 mg/1	500 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-746-05)
51991-746-06	51991-746	HUMAN PRESCRIPTION DRUG	Duloxetine Delayed-Release	DULOXETINE HYDROCHLORIDE	CAPSULE, DELAYED RELEASE PELLETS	ORAL	20140611	N/A	ANDA	ANDA203088	Breckenridge Pharmaceutical, Inc.	DULOXETINE HYDROCHLORIDE	20 mg/1	60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-746-06)
51991-746-90	51991-746	HUMAN PRESCRIPTION DRUG	Duloxetine Delayed-Release	DULOXETINE HYDROCHLORIDE	CAPSULE, DELAYED RELEASE PELLETS	ORAL	20140611	N/A	ANDA	ANDA203088	Breckenridge Pharmaceutical, Inc.	DULOXETINE HYDROCHLORIDE	20 mg/1	90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-746-90)
51991-747-10	51991-747	HUMAN PRESCRIPTION DRUG	Duloxetine Delayed-Release	DULOXETINE HYDROCHLORIDE	CAPSULE, DELAYED RELEASE PELLETS	ORAL	20140611	N/A	ANDA	ANDA203088	Breckenridge Pharmaceutical, Inc.	DULOXETINE HYDROCHLORIDE	30 mg/1	1000 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-747-10)
51991-747-33	51991-747	HUMAN PRESCRIPTION DRUG	Duloxetine Delayed-Release	DULOXETINE HYDROCHLORIDE	CAPSULE, DELAYED RELEASE PELLETS	ORAL	20140611	N/A	ANDA	ANDA203088	Breckenridge Pharmaceutical, Inc.	DULOXETINE HYDROCHLORIDE	30 mg/1	30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-747-33)
51991-747-90	51991-747	HUMAN PRESCRIPTION DRUG	Duloxetine Delayed-Release	DULOXETINE HYDROCHLORIDE	CAPSULE, DELAYED RELEASE PELLETS	ORAL	20140611	N/A	ANDA	ANDA203088	Breckenridge Pharmaceutical, Inc.	DULOXETINE HYDROCHLORIDE	30 mg/1	90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-747-90)
51991-748-10	51991-748	HUMAN PRESCRIPTION DRUG	Duloxetine Delayed-Release	DULOXETINE HYDROCHLORIDE	CAPSULE, DELAYED RELEASE PELLETS	ORAL	20140611	N/A	ANDA	ANDA203088	Breckenridge Pharmaceutical, Inc.	DULOXETINE HYDROCHLORIDE	60 mg/1	1000 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-748-10)
51991-748-33	51991-748	HUMAN PRESCRIPTION DRUG	Duloxetine Delayed-Release	DULOXETINE HYDROCHLORIDE	CAPSULE, DELAYED RELEASE PELLETS	ORAL	20140611	N/A	ANDA	ANDA203088	Breckenridge Pharmaceutical, Inc.	DULOXETINE HYDROCHLORIDE	60 mg/1	30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-748-33)
51991-748-90	51991-748	HUMAN PRESCRIPTION DRUG	Duloxetine Delayed-Release	DULOXETINE HYDROCHLORIDE	CAPSULE, DELAYED RELEASE PELLETS	ORAL	20140611	N/A	ANDA	ANDA203088	Breckenridge Pharmaceutical, Inc.	DULOXETINE HYDROCHLORIDE	60 mg/1	90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-748-90)
51991-750-05	51991-750	HUMAN PRESCRIPTION DRUG	Duloxetine Delayed-Release	DULOXETINE HYDROCHLORIDE	CAPSULE, DELAYED RELEASE PELLETS	ORAL	20180521	N/A	ANDA	ANDA203088	Breckenridge Pharmaceutical, Inc.	DULOXETINE HYDROCHLORIDE	40 mg/1	500 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-750-05)
51991-750-10	51991-750	HUMAN PRESCRIPTION DRUG	Duloxetine Delayed-Release	DULOXETINE HYDROCHLORIDE	CAPSULE, DELAYED RELEASE PELLETS	ORAL	20180521	N/A	ANDA	ANDA203088	Breckenridge Pharmaceutical, Inc.	DULOXETINE HYDROCHLORIDE	40 mg/1	1000 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-750-10)
51991-750-33	51991-750	HUMAN PRESCRIPTION DRUG	Duloxetine Delayed-Release	DULOXETINE HYDROCHLORIDE	CAPSULE, DELAYED RELEASE PELLETS	ORAL	20180521	N/A	ANDA	ANDA203088	Breckenridge Pharmaceutical, Inc.	DULOXETINE HYDROCHLORIDE	40 mg/1	30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-750-33)
51991-750-90	51991-750	HUMAN PRESCRIPTION DRUG	Duloxetine Delayed-Release	DULOXETINE HYDROCHLORIDE	CAPSULE, DELAYED RELEASE PELLETS	ORAL	20180521	N/A	ANDA	ANDA203088	Breckenridge Pharmaceutical, Inc.	DULOXETINE HYDROCHLORIDE	40 mg/1	90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-750-90)
82804-024-30	82804-024	HUMAN PRESCRIPTION DRUG	Duloxetine Delayed-Release	DULOXETINE HYDROCHLORIDE	CAPSULE, DELAYED RELEASE PELLETS	ORAL	20231016	N/A	ANDA	ANDA203088	Proficient Rx LP	DULOXETINE HYDROCHLORIDE	40 mg/1	30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (82804-024-30)
82804-024-60	82804-024	HUMAN PRESCRIPTION DRUG	Duloxetine Delayed-Release	DULOXETINE HYDROCHLORIDE	CAPSULE, DELAYED RELEASE PELLETS	ORAL	20231016	N/A	ANDA	ANDA203088	Proficient Rx LP	DULOXETINE HYDROCHLORIDE	40 mg/1	60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (82804-024-60)
82804-024-90	82804-024	HUMAN PRESCRIPTION DRUG	Duloxetine Delayed-Release	DULOXETINE HYDROCHLORIDE	CAPSULE, DELAYED RELEASE PELLETS	ORAL	20231016	N/A	ANDA	ANDA203088	Proficient Rx LP	DULOXETINE HYDROCHLORIDE	40 mg/1	90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (82804-024-90)
63629-1990-1	63629-1990	HUMAN PRESCRIPTION DRUG	Duloxetine Delayed-Release	DULOXETINE HYDROCHLORIDE	CAPSULE, DELAYED RELEASE PELLETS	ORAL	20140611	N/A	ANDA	ANDA203088	Bryant Ranch Prepack	DULOXETINE HYDROCHLORIDE	20 mg/1	90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (63629-1990-1)