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
59651-309-01	59651-309	HUMAN PRESCRIPTION DRUG	Fluoxetine	Fluoxetine	TABLET, FILM COATED	ORAL	20200408	N/A	ANDA	ANDA213286	Aurobindo Pharma Limited	FLUOXETINE HYDROCHLORIDE	20 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (59651-309-01)
59651-308-30	59651-308	HUMAN PRESCRIPTION DRUG	Fluoxetine	Fluoxetine	TABLET, FILM COATED	ORAL	20200408	N/A	ANDA	ANDA213286	Aurobindo Pharma Limited	FLUOXETINE HYDROCHLORIDE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (59651-308-30)
59651-308-01	59651-308	HUMAN PRESCRIPTION DRUG	Fluoxetine	Fluoxetine	TABLET, FILM COATED	ORAL	20200408	N/A	ANDA	ANDA213286	Aurobindo Pharma Limited	FLUOXETINE HYDROCHLORIDE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (59651-308-01)
59651-309-30	59651-309	HUMAN PRESCRIPTION DRUG	Fluoxetine	Fluoxetine	TABLET, FILM COATED	ORAL	20200408	N/A	ANDA	ANDA213286	Aurobindo Pharma Limited	FLUOXETINE HYDROCHLORIDE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (59651-309-30)
70518-4428-0	70518-4428	HUMAN PRESCRIPTION DRUG	Fluoxetine	Fluoxetine	TABLET, FILM COATED	ORAL	20250806	N/A	ANDA	ANDA213286	REMEDYREPACK INC.	FLUOXETINE HYDROCHLORIDE	20 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4428-0)
70518-4429-0	70518-4429	HUMAN PRESCRIPTION DRUG	Fluoxetine	Fluoxetine	TABLET, FILM COATED	ORAL	20250808	N/A	ANDA	ANDA213286	REMEDYREPACK INC.	FLUOXETINE HYDROCHLORIDE	10 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4429-0)
71335-2778-2	71335-2778	HUMAN PRESCRIPTION DRUG	Fluoxetine	Fluoxetine	TABLET, FILM COATED	ORAL	20251013	N/A	ANDA	ANDA213286	Bryant Ranch Prepack	FLUOXETINE HYDROCHLORIDE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (71335-2778-2)
71335-2778-1	71335-2778	HUMAN PRESCRIPTION DRUG	Fluoxetine	Fluoxetine	TABLET, FILM COATED	ORAL	20251013	N/A	ANDA	ANDA213286	Bryant Ranch Prepack	FLUOXETINE HYDROCHLORIDE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-2778-1)
71335-2784-1	71335-2784	HUMAN PRESCRIPTION DRUG	Fluoxetine	Fluoxetine	TABLET, FILM COATED	ORAL	20250818	N/A	ANDA	ANDA213286	Bryant Ranch Prepack	FLUOXETINE HYDROCHLORIDE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-2784-1)
71335-2784-2	71335-2784	HUMAN PRESCRIPTION DRUG	Fluoxetine	Fluoxetine	TABLET, FILM COATED	ORAL	20250818	N/A	ANDA	ANDA213286	Bryant Ranch Prepack	FLUOXETINE HYDROCHLORIDE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (71335-2784-2)