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
59651-530-03	59651-530	HUMAN PRESCRIPTION DRUG	Erlotinib	Erlotinib	TABLET, FILM COATED	ORAL	20220622	N/A	ANDA	ANDA216342	Aurobindo Pharma Limited	ERLOTINIB HYDROCHLORIDE	25 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (59651-530-03)
59651-530-10	59651-530	HUMAN PRESCRIPTION DRUG	Erlotinib	Erlotinib	TABLET, FILM COATED	ORAL	20220622	N/A	ANDA	ANDA216342	Aurobindo Pharma Limited	ERLOTINIB HYDROCHLORIDE	25 mg/1	1 BLISTER PACK in 1 CARTON (59651-530-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK
59651-531-03	59651-531	HUMAN PRESCRIPTION DRUG	Erlotinib	Erlotinib	TABLET, FILM COATED	ORAL	20220622	N/A	ANDA	ANDA216342	Aurobindo Pharma Limited	ERLOTINIB HYDROCHLORIDE	100 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (59651-531-03)
59651-531-10	59651-531	HUMAN PRESCRIPTION DRUG	Erlotinib	Erlotinib	TABLET, FILM COATED	ORAL	20220622	N/A	ANDA	ANDA216342	Aurobindo Pharma Limited	ERLOTINIB HYDROCHLORIDE	100 mg/1	1 BLISTER PACK in 1 CARTON (59651-531-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK
59651-532-03	59651-532	HUMAN PRESCRIPTION DRUG	Erlotinib	Erlotinib	TABLET, FILM COATED	ORAL	20220622	N/A	ANDA	ANDA216342	Aurobindo Pharma Limited	ERLOTINIB HYDROCHLORIDE	150 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (59651-532-03)
59651-532-10	59651-532	HUMAN PRESCRIPTION DRUG	Erlotinib	Erlotinib	TABLET, FILM COATED	ORAL	20220622	N/A	ANDA	ANDA216342	Aurobindo Pharma Limited	ERLOTINIB HYDROCHLORIDE	150 mg/1	1 BLISTER PACK in 1 CARTON (59651-532-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK