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
68071-1640-3	68071-1640	HUMAN PRESCRIPTION DRUG	Terbinafine Hydrochloride	Terbinafine Hydrochloride	TABLET	ORAL	20171102	N/A	ANDA	ANDA077137	NuCare Pharmaceuticals,Inc.	TERBINAFINE HYDROCHLORIDE	250 mg/1	30 TABLET in 1 BOTTLE (68071-1640-3)
69097-731-07	69097-731	HUMAN PRESCRIPTION DRUG	TERBINAFINE HYDROCHLORIDE	Terbinafine Tablets 250 mg	TABLET	ORAL	20210108	N/A	ANDA	ANDA077137	Cipla USA Inc.	TERBINAFINE HYDROCHLORIDE	250 mg/1	100 TABLET in 1 BOTTLE (69097-731-07)
69097-731-02	69097-731	HUMAN PRESCRIPTION DRUG	TERBINAFINE HYDROCHLORIDE	Terbinafine Tablets 250 mg	TABLET	ORAL	20210108	N/A	ANDA	ANDA077137	Cipla USA Inc.	TERBINAFINE HYDROCHLORIDE	250 mg/1	30 TABLET in 1 BOTTLE (69097-731-02)
68071-2381-3	68071-2381	HUMAN PRESCRIPTION DRUG	TERBINAFINE HYDROCHLORIDE	Terbinafine Tablets 250 mg	TABLET	ORAL	20210402	N/A	ANDA	ANDA077137	NuCare Pharmaceuticals,Inc.	TERBINAFINE HYDROCHLORIDE	250 mg/1	30 TABLET in 1 BOTTLE (68071-2381-3)