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
62332-242-30	62332-242	HUMAN PRESCRIPTION DRUG	Fluoxetine	Fluoxetine	TABLET, FILM COATED	ORAL	20170407	N/A	ANDA	ANDA208698	Alembic Pharmaceuticals Inc.	FLUOXETINE HYDROCHLORIDE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (62332-242-30)
62332-242-31	62332-242	HUMAN PRESCRIPTION DRUG	Fluoxetine	Fluoxetine	TABLET, FILM COATED	ORAL	20170407	N/A	ANDA	ANDA208698	Alembic Pharmaceuticals Inc.	FLUOXETINE HYDROCHLORIDE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (62332-242-31)
62332-242-91	62332-242	HUMAN PRESCRIPTION DRUG	Fluoxetine	Fluoxetine	TABLET, FILM COATED	ORAL	20170407	N/A	ANDA	ANDA208698	Alembic Pharmaceuticals Inc.	FLUOXETINE HYDROCHLORIDE	10 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (62332-242-91)
62332-243-30	62332-243	HUMAN PRESCRIPTION DRUG	Fluoxetine	Fluoxetine	TABLET, FILM COATED	ORAL	20170407	N/A	ANDA	ANDA208698	Alembic Pharmaceuticals Inc.	FLUOXETINE HYDROCHLORIDE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (62332-243-30)
62332-243-31	62332-243	HUMAN PRESCRIPTION DRUG	Fluoxetine	Fluoxetine	TABLET, FILM COATED	ORAL	20170407	N/A	ANDA	ANDA208698	Alembic Pharmaceuticals Inc.	FLUOXETINE HYDROCHLORIDE	20 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (62332-243-31)
62332-243-91	62332-243	HUMAN PRESCRIPTION DRUG	Fluoxetine	Fluoxetine	TABLET, FILM COATED	ORAL	20170407	N/A	ANDA	ANDA208698	Alembic Pharmaceuticals Inc.	FLUOXETINE HYDROCHLORIDE	20 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (62332-243-91)
46708-242-30	46708-242	HUMAN PRESCRIPTION DRUG	Fluoxetine Hydrochloride	Fluoxetine Hydrochloride	TABLET, FILM COATED	ORAL	20170415	N/A	ANDA	ANDA208698	Alembic Pharmaceuticals Limited	FLUOXETINE HYDROCHLORIDE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (46708-242-30)
46708-242-31	46708-242	HUMAN PRESCRIPTION DRUG	Fluoxetine Hydrochloride	Fluoxetine Hydrochloride	TABLET, FILM COATED	ORAL	20170415	N/A	ANDA	ANDA208698	Alembic Pharmaceuticals Limited	FLUOXETINE HYDROCHLORIDE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (46708-242-31)
46708-242-91	46708-242	HUMAN PRESCRIPTION DRUG	Fluoxetine Hydrochloride	Fluoxetine Hydrochloride	TABLET, FILM COATED	ORAL	20170415	N/A	ANDA	ANDA208698	Alembic Pharmaceuticals Limited	FLUOXETINE HYDROCHLORIDE	10 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (46708-242-91)
46708-243-30	46708-243	HUMAN PRESCRIPTION DRUG	Fluoxetine Hydrochloride	Fluoxetine Hydrochloride	TABLET, FILM COATED	ORAL	20170415	N/A	ANDA	ANDA208698	Alembic Pharmaceuticals Limited	FLUOXETINE HYDROCHLORIDE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (46708-243-30)
46708-243-31	46708-243	HUMAN PRESCRIPTION DRUG	Fluoxetine Hydrochloride	Fluoxetine Hydrochloride	TABLET, FILM COATED	ORAL	20170415	N/A	ANDA	ANDA208698	Alembic Pharmaceuticals Limited	FLUOXETINE HYDROCHLORIDE	20 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (46708-243-31)
46708-243-91	46708-243	HUMAN PRESCRIPTION DRUG	Fluoxetine Hydrochloride	Fluoxetine Hydrochloride	TABLET, FILM COATED	ORAL	20170415	N/A	ANDA	ANDA208698	Alembic Pharmaceuticals Limited	FLUOXETINE HYDROCHLORIDE	20 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (46708-243-91)