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
72162-1597-5	72162-1597	HUMAN PRESCRIPTION DRUG	Duloxetine Delayed-Release	DULOXETINE HYDROCHLORIDE	CAPSULE, DELAYED RELEASE PELLETS	ORAL	20240205	N/A	ANDA	ANDA203088	Bryant Ranch Prepack	DULOXETINE HYDROCHLORIDE	20 mg/1	500 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (72162-1597-5)
72162-1597-9	72162-1597	HUMAN PRESCRIPTION DRUG	Duloxetine Delayed-Release	DULOXETINE HYDROCHLORIDE	CAPSULE, DELAYED RELEASE PELLETS	ORAL	20240205	N/A	ANDA	ANDA203088	Bryant Ranch Prepack	DULOXETINE HYDROCHLORIDE	20 mg/1	90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (72162-1597-9)
72162-1598-9	72162-1598	HUMAN PRESCRIPTION DRUG	Duloxetine Delayed-Release	DULOXETINE HYDROCHLORIDE	CAPSULE, DELAYED RELEASE PELLETS	ORAL	20240205	N/A	ANDA	ANDA203088	Bryant Ranch Prepack	DULOXETINE HYDROCHLORIDE	30 mg/1	90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (72162-1598-9)
72162-1599-1	72162-1599	HUMAN PRESCRIPTION DRUG	Duloxetine Delayed-Release	DULOXETINE HYDROCHLORIDE	CAPSULE, DELAYED RELEASE PELLETS	ORAL	20240205	N/A	ANDA	ANDA203088	Bryant Ranch Prepack	DULOXETINE HYDROCHLORIDE	60 mg/1	100 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (72162-1599-1)
72162-1599-9	72162-1599	HUMAN PRESCRIPTION DRUG	Duloxetine Delayed-Release	DULOXETINE HYDROCHLORIDE	CAPSULE, DELAYED RELEASE PELLETS	ORAL	20240205	N/A	ANDA	ANDA203088	Bryant Ranch Prepack	DULOXETINE HYDROCHLORIDE	60 mg/1	90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (72162-1599-9)
72162-1600-3	72162-1600	HUMAN PRESCRIPTION DRUG	Duloxetine Delayed-Release	DULOXETINE HYDROCHLORIDE	CAPSULE, DELAYED RELEASE PELLETS	ORAL	20180521	N/A	ANDA	ANDA203088	Bryant Ranch Prepack	DULOXETINE HYDROCHLORIDE	40 mg/1	30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (72162-1600-3)
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)
63187-702-30	63187-702	HUMAN PRESCRIPTION DRUG	DULOXETINE DELAYED-RELEASE	DULOXETINE HYDROCHLORIDE	CAPSULE, DELAYED RELEASE PELLETS	ORAL	20160502	N/A	ANDA	ANDA203088	Proficient Rx LP	DULOXETINE HYDROCHLORIDE	30 mg/1	30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (63187-702-30)