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
0832-0111-00	0832-0111	HUMAN PRESCRIPTION DRUG	Amantadine Hydrochloride	amantadine hydrochloride	TABLET	ORAL	20111215	N/A	ANDA	ANDA076186	Upsher-Smith Laboratories, LLC	AMANTADINE HYDROCHLORIDE	100 mg/1	100 TABLET in 1 BOTTLE (0832-0111-00)
0832-0111-03	0832-0111	HUMAN PRESCRIPTION DRUG	Amantadine Hydrochloride	amantadine hydrochloride	TABLET	ORAL	20170707	N/A	ANDA	ANDA076186	Upsher-Smith Laboratories, LLC	AMANTADINE HYDROCHLORIDE	100 mg/1	100 BLISTER PACK in 1 CARTON (0832-0111-03) / 1 TABLET in 1 BLISTER PACK (0832-0111-89)
0832-0111-50	0832-0111	HUMAN PRESCRIPTION DRUG	Amantadine Hydrochloride	amantadine hydrochloride	TABLET	ORAL	20111215	N/A	ANDA	ANDA076186	Upsher-Smith Laboratories, LLC	AMANTADINE HYDROCHLORIDE	100 mg/1	500 TABLET in 1 BOTTLE (0832-0111-50)
70518-3381-0	70518-3381	HUMAN PRESCRIPTION DRUG	Amantadine Hydrochloride	amantadine hydrochloride	TABLET	ORAL	20220310	N/A	ANDA	ANDA076186	REMEDYREPACK INC.	AMANTADINE HYDROCHLORIDE	100 mg/1	100 POUCH in 1 BOX (70518-3381-0) / 1 TABLET in 1 POUCH (70518-3381-1)