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
71335-1145-3	71335-1145	HUMAN PRESCRIPTION DRUG	Fluoxetine	Fluoxetine Hydrochloride	CAPSULE	ORAL	20190321	N/A	ANDA	ANDA078619	Bryant Ranch Prepack	FLUOXETINE HYDROCHLORIDE	40 mg/1	100 CAPSULE in 1 BOTTLE (71335-1145-3)
71335-1145-4	71335-1145	HUMAN PRESCRIPTION DRUG	Fluoxetine	Fluoxetine Hydrochloride	CAPSULE	ORAL	20190312	N/A	ANDA	ANDA078619	Bryant Ranch Prepack	FLUOXETINE HYDROCHLORIDE	40 mg/1	90 CAPSULE in 1 BOTTLE (71335-1145-4)
71335-1145-5	71335-1145	HUMAN PRESCRIPTION DRUG	Fluoxetine	Fluoxetine Hydrochloride	CAPSULE	ORAL	20240517	N/A	ANDA	ANDA078619	Bryant Ranch Prepack	FLUOXETINE HYDROCHLORIDE	40 mg/1	28 CAPSULE in 1 BOTTLE (71335-1145-5)
71335-1145-6	71335-1145	HUMAN PRESCRIPTION DRUG	Fluoxetine	Fluoxetine Hydrochloride	CAPSULE	ORAL	20240517	N/A	ANDA	ANDA078619	Bryant Ranch Prepack	FLUOXETINE HYDROCHLORIDE	40 mg/1	180 CAPSULE in 1 BOTTLE (71335-1145-6)
71335-1145-7	71335-1145	HUMAN PRESCRIPTION DRUG	Fluoxetine	Fluoxetine Hydrochloride	CAPSULE	ORAL	20240517	N/A	ANDA	ANDA078619	Bryant Ranch Prepack	FLUOXETINE HYDROCHLORIDE	40 mg/1	120 CAPSULE in 1 BOTTLE (71335-1145-7)
72189-067-30	72189-067	HUMAN PRESCRIPTION DRUG	FLUOXETINE	FLUOXETINE HYDROCHLORIDE	CAPSULE	ORAL	20200107	N/A	ANDA	ANDA078619	DIRECT RX	FLUOXETINE HYDROCHLORIDE	40 mg/1	30 CAPSULE in 1 BOTTLE (72189-067-30)
72189-067-90	72189-067	HUMAN PRESCRIPTION DRUG	FLUOXETINE	FLUOXETINE HYDROCHLORIDE	CAPSULE	ORAL	20200107	N/A	ANDA	ANDA078619	DIRECT RX	FLUOXETINE HYDROCHLORIDE	40 mg/1	90 CAPSULE in 1 BOTTLE (72189-067-90)
82009-101-10	82009-101	HUMAN PRESCRIPTION DRUG	Fluoxetine	Fluoxetine Hydrochloride	CAPSULE	ORAL	20230901	N/A	ANDA	ANDA078619	QUALLENT PHARMACEUTICALS HEALTH LLC	FLUOXETINE HYDROCHLORIDE	20 mg/1	1000 CAPSULE in 1 BOTTLE (82009-101-10)
82009-102-05	82009-102	HUMAN PRESCRIPTION DRUG	Fluoxetine	Fluoxetine Hydrochloride	CAPSULE	ORAL	20230901	N/A	ANDA	ANDA078619	QUALLENT PHARMACEUTICALS HEALTH LLC	FLUOXETINE HYDROCHLORIDE	40 mg/1	500 CAPSULE in 1 BOTTLE (82009-102-05)