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
72205-080-30	72205-080	HUMAN PRESCRIPTION DRUG	Erlotinib Hydrochloride	Erlotinib Hydrochloride	TABLET, FILM COATED	ORAL	20210511	N/A	ANDA	ANDA214366	Novadoz Pharmaceuticals LLC	ERLOTINIB HYDROCHLORIDE	25 mg/1	1 BOTTLE in 1 CARTON (72205-080-30) / 30 TABLET, FILM COATED in 1 BOTTLE
72205-081-30	72205-081	HUMAN PRESCRIPTION DRUG	Erlotinib Hydrochloride	Erlotinib Hydrochloride	TABLET, FILM COATED	ORAL	20210511	N/A	ANDA	ANDA214366	Novadoz Pharmaceuticals LLC	ERLOTINIB HYDROCHLORIDE	100 mg/1	1 BOTTLE in 1 CARTON (72205-081-30) / 30 TABLET, FILM COATED in 1 BOTTLE
72205-082-30	72205-082	HUMAN PRESCRIPTION DRUG	Erlotinib Hydrochloride	Erlotinib Hydrochloride	TABLET, FILM COATED	ORAL	20210511	N/A	ANDA	ANDA214366	Novadoz Pharmaceuticals LLC	ERLOTINIB HYDROCHLORIDE	150 mg/1	1 BOTTLE in 1 CARTON (72205-082-30) / 30 TABLET, FILM COATED in 1 BOTTLE
69539-090-30	69539-090	HUMAN PRESCRIPTION DRUG	Erlotinib Hydrochloride	Erlotinib Hydrochloride	TABLET, FILM COATED	ORAL	20210511	N/A	ANDA	ANDA214366	MSN LABORATORIES PRIVATE LIMITED	ERLOTINIB HYDROCHLORIDE	25 mg/1	1 BOTTLE in 1 CARTON (69539-090-30) / 30 TABLET, FILM COATED in 1 BOTTLE
69539-091-30	69539-091	HUMAN PRESCRIPTION DRUG	Erlotinib Hydrochloride	Erlotinib Hydrochloride	TABLET, FILM COATED	ORAL	20210511	N/A	ANDA	ANDA214366	MSN LABORATORIES PRIVATE LIMITED	ERLOTINIB HYDROCHLORIDE	100 mg/1	1 BOTTLE in 1 CARTON (69539-091-30) / 30 TABLET, FILM COATED in 1 BOTTLE
69539-092-30	69539-092	HUMAN PRESCRIPTION DRUG	Erlotinib Hydrochloride	Erlotinib Hydrochloride	TABLET, FILM COATED	ORAL	20210511	N/A	ANDA	ANDA214366	MSN LABORATORIES PRIVATE LIMITED	ERLOTINIB HYDROCHLORIDE	150 mg/1	1 BOTTLE in 1 CARTON (69539-092-30) / 30 TABLET, FILM COATED in 1 BOTTLE