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
62332-023-71	62332-023	HUMAN PRESCRIPTION DRUG	Fluoxetine	Fluoxetine	CAPSULE	ORAL	20160129	N/A	ANDA	ANDA090223	Alembic Pharmaceuticals Inc.	FLUOXETINE HYDROCHLORIDE	20 mg/1	500 CAPSULE in 1 BOTTLE (62332-023-71)
62332-023-91	62332-023	HUMAN PRESCRIPTION DRUG	Fluoxetine	Fluoxetine	CAPSULE	ORAL	20160129	N/A	ANDA	ANDA090223	Alembic Pharmaceuticals Inc.	FLUOXETINE HYDROCHLORIDE	20 mg/1	1000 CAPSULE in 1 BOTTLE (62332-023-91)
46708-272-30	46708-272	HUMAN PRESCRIPTION DRUG	Fluoxetine	Fluoxetine	CAPSULE	ORAL	20090701	N/A	ANDA	ANDA090223	Alembic Pharmaceuticals Limited	FLUOXETINE HYDROCHLORIDE	20 mg/1	30 CAPSULE in 1 BOTTLE (46708-272-30)
46708-272-31	46708-272	HUMAN PRESCRIPTION DRUG	Fluoxetine	Fluoxetine	CAPSULE	ORAL	20090701	N/A	ANDA	ANDA090223	Alembic Pharmaceuticals Limited	FLUOXETINE HYDROCHLORIDE	20 mg/1	100 CAPSULE in 1 BOTTLE (46708-272-31)
46708-272-71	46708-272	HUMAN PRESCRIPTION DRUG	Fluoxetine	Fluoxetine	CAPSULE	ORAL	20090701	N/A	ANDA	ANDA090223	Alembic Pharmaceuticals Limited	FLUOXETINE HYDROCHLORIDE	20 mg/1	500 CAPSULE in 1 BOTTLE (46708-272-71)
46708-272-91	46708-272	HUMAN PRESCRIPTION DRUG	Fluoxetine	Fluoxetine	CAPSULE	ORAL	20090701	N/A	ANDA	ANDA090223	Alembic Pharmaceuticals Limited	FLUOXETINE HYDROCHLORIDE	20 mg/1	1000 CAPSULE in 1 BOTTLE (46708-272-91)