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
55111-250-79	55111-250	HUMAN PRESCRIPTION DRUG	Terbinafine Hydrochloride	Terbinafine Hydrochloride	TABLET	ORAL	20070702	N/A	ANDA	ANDA076390	Dr.Reddys Laboratories Limited	TERBINAFINE HYDROCHLORIDE	250 mg/1	10 BLISTER PACK in 1 CARTON (55111-250-79) / 10 TABLET in 1 BLISTER PACK (55111-250-78)
55111-250-90	55111-250	HUMAN PRESCRIPTION DRUG	Terbinafine Hydrochloride	Terbinafine Hydrochloride	TABLET	ORAL	20070702	N/A	ANDA	ANDA076390	Dr.Reddys Laboratories Limited	TERBINAFINE HYDROCHLORIDE	250 mg/1	90 TABLET in 1 BOTTLE (55111-250-90)
55111-250-30	55111-250	HUMAN PRESCRIPTION DRUG	Terbinafine Hydrochloride	Terbinafine Hydrochloride	TABLET	ORAL	20070702	N/A	ANDA	ANDA076390	Dr.Reddys Laboratories Limited	TERBINAFINE HYDROCHLORIDE	250 mg/1	30 TABLET in 1 BOTTLE (55111-250-30)
55111-250-05	55111-250	HUMAN PRESCRIPTION DRUG	Terbinafine Hydrochloride	Terbinafine Hydrochloride	TABLET	ORAL	20070702	N/A	ANDA	ANDA076390	Dr.Reddys Laboratories Limited	TERBINAFINE HYDROCHLORIDE	250 mg/1	500 TABLET in 1 BOTTLE (55111-250-05)
55111-250-01	55111-250	HUMAN PRESCRIPTION DRUG	Terbinafine Hydrochloride	Terbinafine Hydrochloride	TABLET	ORAL	20070702	N/A	ANDA	ANDA076390	Dr.Reddys Laboratories Limited	TERBINAFINE HYDROCHLORIDE	250 mg/1	100 TABLET in 1 BOTTLE (55111-250-01)