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
0093-8119-56	0093-8119	HUMAN PRESCRIPTION DRUG	Famciclovir	Famciclovir	TABLET, FILM COATED	ORAL	20070905	N/A	ANDA	ANDA077487	Teva Pharmaceuticals USA, Inc.	FAMCICLOVIR	500 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0093-8119-56)
42291-414-30	42291-414	HUMAN PRESCRIPTION DRUG	Famciclovir	Famciclovir	TABLET, FILM COATED	ORAL	20210519	N/A	ANDA	ANDA077487	AvKARE	FAMCICLOVIR	125 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (42291-414-30)
42291-415-30	42291-415	HUMAN PRESCRIPTION DRUG	Famciclovir	Famciclovir	TABLET, FILM COATED	ORAL	20210519	N/A	ANDA	ANDA077487	AvKARE	FAMCICLOVIR	250 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (42291-415-30)
42291-416-30	42291-416	HUMAN PRESCRIPTION DRUG	Famciclovir	Famciclovir	TABLET, FILM COATED	ORAL	20210519	N/A	ANDA	ANDA077487	AvKARE	FAMCICLOVIR	500 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (42291-416-30)
55289-168-03	55289-168	HUMAN PRESCRIPTION DRUG	Famciclovir	Famciclovir	TABLET, FILM COATED	ORAL	20110414	N/A	ANDA	ANDA077487	PD-Rx Pharmaceuticals, Inc.	FAMCICLOVIR	500 mg/1	3 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-168-03)
0093-8118-56	0093-8118	HUMAN PRESCRIPTION DRUG	Famciclovir	Famciclovir	TABLET, FILM COATED	ORAL	20070905	N/A	ANDA	ANDA077487	Teva Pharmaceuticals USA, Inc.	FAMCICLOVIR	250 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0093-8118-56)
0093-8117-56	0093-8117	HUMAN PRESCRIPTION DRUG	Famciclovir	Famciclovir	TABLET, FILM COATED	ORAL	20070905	N/A	ANDA	ANDA077487	Teva Pharmaceuticals USA, Inc.	FAMCICLOVIR	125 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0093-8117-56)