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
59923-725-30	59923-725	HUMAN PRESCRIPTION DRUG	Erlotinib	Erlotinib	TABLET, FILM COATED	ORAL	20200501	N/A	ANDA	ANDA211960	Areva Pharmaceuticals	ERLOTINIB HYDROCHLORIDE	25 mg/1	1 BOTTLE in 1 BOX (59923-725-30) / 30 TABLET, FILM COATED in 1 BOTTLE
59923-726-30	59923-726	HUMAN PRESCRIPTION DRUG	Erlotinib	Erlotinib	TABLET, FILM COATED	ORAL	20200501	N/A	ANDA	ANDA211960	Areva Pharmaceuticals	ERLOTINIB HYDROCHLORIDE	100 mg/1	1 BOTTLE in 1 BOX (59923-726-30) / 30 TABLET, FILM COATED in 1 BOTTLE
59923-727-30	59923-727	HUMAN PRESCRIPTION DRUG	Erlotinib	Erlotinib	TABLET, FILM COATED	ORAL	20200501	N/A	ANDA	ANDA211960	Areva Pharmaceuticals	ERLOTINIB HYDROCHLORIDE	150 mg/1	1 BOTTLE in 1 BOX (59923-727-30) / 30 TABLET, FILM COATED in 1 BOTTLE
72485-219-30	72485-219	HUMAN PRESCRIPTION DRUG	Erlotinib	Erlotinib hydrochloride	TABLET, FILM COATED	ORAL	20191106	N/A	ANDA	ANDA211960	Armas Pharmaceuticals Inc.	ERLOTINIB HYDROCHLORIDE	150 mg/1	1 BOTTLE in 1 BOX (72485-219-30) / 30 TABLET, FILM COATED in 1 BOTTLE
72485-218-30	72485-218	HUMAN PRESCRIPTION DRUG	Erlotinib	Erlotinib hydrochloride	TABLET, FILM COATED	ORAL	20191106	N/A	ANDA	ANDA211960	Armas Pharmaceuticals Inc.	ERLOTINIB HYDROCHLORIDE	100 mg/1	1 BOTTLE in 1 BOX (72485-218-30) / 30 TABLET, FILM COATED in 1 BOTTLE
72485-217-30	72485-217	HUMAN PRESCRIPTION DRUG	Erlotinib	Erlotinib hydrochloride	TABLET, FILM COATED	ORAL	20191106	N/A	ANDA	ANDA211960	Armas Pharmaceuticals Inc.	ERLOTINIB HYDROCHLORIDE	25 mg/1	1 BOTTLE in 1 BOX (72485-217-30) / 30 TABLET, FILM COATED in 1 BOTTLE