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
63304-096-30	63304-096	HUMAN PRESCRIPTION DRUG	Erlotinib	Erlotinib	TABLET, FILM COATED	ORAL	20191105	N/A	ANDA	ANDA210300	Sun Pharmaceutical Industries, Inc.	ERLOTINIB	100 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (63304-096-30)
63304-096-11	63304-096	HUMAN PRESCRIPTION DRUG	Erlotinib	Erlotinib	TABLET, FILM COATED	ORAL	20191105	N/A	ANDA	ANDA210300	Sun Pharmaceutical Industries, Inc.	ERLOTINIB	100 mg/1	3 BLISTER PACK in 1 CARTON (63304-096-11) / 10 TABLET, FILM COATED in 1 BLISTER PACK (63304-096-31)
63304-095-30	63304-095	HUMAN PRESCRIPTION DRUG	Erlotinib	Erlotinib	TABLET, FILM COATED	ORAL	20191105	N/A	ANDA	ANDA210300	Sun Pharmaceutical Industries, Inc.	ERLOTINIB	25 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (63304-095-30)
63304-095-11	63304-095	HUMAN PRESCRIPTION DRUG	Erlotinib	Erlotinib	TABLET, FILM COATED	ORAL	20191105	N/A	ANDA	ANDA210300	Sun Pharmaceutical Industries, Inc.	ERLOTINIB	25 mg/1	3 BLISTER PACK in 1 CARTON (63304-095-11) / 10 TABLET, FILM COATED in 1 BLISTER PACK (63304-095-31)
63304-135-11	63304-135	HUMAN PRESCRIPTION DRUG	Erlotinib	Erlotinib	TABLET, FILM COATED	ORAL	20191105	N/A	ANDA	ANDA210300	Sun Pharmaceutical Industries, Inc.	ERLOTINIB	150 mg/1	3 BLISTER PACK in 1 CARTON (63304-135-11) / 10 TABLET, FILM COATED in 1 BLISTER PACK (63304-135-31)
63304-135-30	63304-135	HUMAN PRESCRIPTION DRUG	Erlotinib	Erlotinib	TABLET, FILM COATED	ORAL	20191105	N/A	ANDA	ANDA210300	Sun Pharmaceutical Industries, Inc.	ERLOTINIB	150 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (63304-135-30)