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
75907-058-10	75907-058	HUMAN PRESCRIPTION DRUG	Tamoxifen Citrate	Tamoxifen Citrate	TABLET, FILM COATED	ORAL	20240822	N/A	ANDA	ANDA075797	Dr. Reddy's Labratories Inc.	TAMOXIFEN CITRATE	10 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (75907-058-10)
75907-058-60	75907-058	HUMAN PRESCRIPTION DRUG	Tamoxifen Citrate	Tamoxifen Citrate	TABLET, FILM COATED	ORAL	20240822	N/A	ANDA	ANDA075797	Dr. Reddy's Labratories Inc.	TAMOXIFEN CITRATE	10 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (75907-058-60)
75907-059-10	75907-059	HUMAN PRESCRIPTION DRUG	Tamoxifen Citrate	Tamoxifen Citrate	TABLET, FILM COATED	ORAL	20240822	N/A	ANDA	ANDA075797	Dr. Reddy's Labratories Inc.	TAMOXIFEN CITRATE	20 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (75907-059-10)
75907-059-30	75907-059	HUMAN PRESCRIPTION DRUG	Tamoxifen Citrate	Tamoxifen Citrate	TABLET, FILM COATED	ORAL	20240822	N/A	ANDA	ANDA075797	Dr. Reddy's Labratories Inc.	TAMOXIFEN CITRATE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (75907-059-30)
51862-643-10	51862-643	HUMAN PRESCRIPTION DRUG	Tamoxifen Citrate	Tamoxifen Citrate	TABLET, FILM COATED	ORAL	20210827	N/A	ANDA	ANDA075797	Mayne Pharma Commercial LLC	TAMOXIFEN CITRATE	20 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (51862-643-10)
51862-643-30	51862-643	HUMAN PRESCRIPTION DRUG	Tamoxifen Citrate	Tamoxifen Citrate	TABLET, FILM COATED	ORAL	20210827	N/A	ANDA	ANDA075797	Mayne Pharma Commercial LLC	TAMOXIFEN CITRATE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (51862-643-30)