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
72578-057-77	72578-057	HUMAN PRESCRIPTION DRUG	Felbamate	Felbamate	TABLET	ORAL	20200303	N/A	ANDA	ANDA208970	Viona Pharmaceuticals Inc	FELBAMATE	600 mg/1	10 BLISTER PACK in 1 CARTON (72578-057-77) / 10 TABLET in 1 BLISTER PACK (72578-057-30)
72578-057-01	72578-057	HUMAN PRESCRIPTION DRUG	Felbamate	Felbamate	TABLET	ORAL	20200303	N/A	ANDA	ANDA208970	Viona Pharmaceuticals Inc	FELBAMATE	600 mg/1	100 TABLET in 1 BOTTLE (72578-057-01)
72578-057-05	72578-057	HUMAN PRESCRIPTION DRUG	Felbamate	Felbamate	TABLET	ORAL	20200303	N/A	ANDA	ANDA208970	Viona Pharmaceuticals Inc	FELBAMATE	600 mg/1	500 TABLET in 1 BOTTLE (72578-057-05)
72578-057-06	72578-057	HUMAN PRESCRIPTION DRUG	Felbamate	Felbamate	TABLET	ORAL	20200303	N/A	ANDA	ANDA208970	Viona Pharmaceuticals Inc	FELBAMATE	600 mg/1	30 TABLET in 1 BOTTLE (72578-057-06)
72578-057-16	72578-057	HUMAN PRESCRIPTION DRUG	Felbamate	Felbamate	TABLET	ORAL	20200303	N/A	ANDA	ANDA208970	Viona Pharmaceuticals Inc	FELBAMATE	600 mg/1	90 TABLET in 1 BOTTLE (72578-057-16)
72578-057-28	72578-057	HUMAN PRESCRIPTION DRUG	Felbamate	Felbamate	TABLET	ORAL	20200303	N/A	ANDA	ANDA208970	Viona Pharmaceuticals Inc	FELBAMATE	600 mg/1	180 TABLET in 1 BOTTLE (72578-057-28)
70771-1077-1	70771-1077	HUMAN PRESCRIPTION DRUG	Felbamate	Felbamate	TABLET	ORAL	20170815	N/A	ANDA	ANDA208970	Zydus Lifesciences Limited	FELBAMATE	400 mg/1	100 TABLET in 1 BOTTLE (70771-1077-1)
70771-1077-3	70771-1077	HUMAN PRESCRIPTION DRUG	Felbamate	Felbamate	TABLET	ORAL	20170815	N/A	ANDA	ANDA208970	Zydus Lifesciences Limited	FELBAMATE	400 mg/1	30 TABLET in 1 BOTTLE (70771-1077-3)
70771-1077-4	70771-1077	HUMAN PRESCRIPTION DRUG	Felbamate	Felbamate	TABLET	ORAL	20170815	N/A	ANDA	ANDA208970	Zydus Lifesciences Limited	FELBAMATE	400 mg/1	10 BLISTER PACK in 1 CARTON (70771-1077-4) / 10 TABLET in 1 BLISTER PACK
70771-1077-5	70771-1077	HUMAN PRESCRIPTION DRUG	Felbamate	Felbamate	TABLET	ORAL	20170815	N/A	ANDA	ANDA208970	Zydus Lifesciences Limited	FELBAMATE	400 mg/1	500 TABLET in 1 BOTTLE (70771-1077-5)
70771-1077-9	70771-1077	HUMAN PRESCRIPTION DRUG	Felbamate	Felbamate	TABLET	ORAL	20170815	N/A	ANDA	ANDA208970	Zydus Lifesciences Limited	FELBAMATE	400 mg/1	90 TABLET in 1 BOTTLE (70771-1077-9)
72578-056-01	72578-056	HUMAN PRESCRIPTION DRUG	Felbamate	Felbamate	TABLET	ORAL	20200303	N/A	ANDA	ANDA208970	Viona Pharmaceuticals Inc	FELBAMATE	400 mg/1	100 TABLET in 1 BOTTLE (72578-056-01)
72578-056-05	72578-056	HUMAN PRESCRIPTION DRUG	Felbamate	Felbamate	TABLET	ORAL	20200303	N/A	ANDA	ANDA208970	Viona Pharmaceuticals Inc	FELBAMATE	400 mg/1	500 TABLET in 1 BOTTLE (72578-056-05)
72578-056-06	72578-056	HUMAN PRESCRIPTION DRUG	Felbamate	Felbamate	TABLET	ORAL	20200303	N/A	ANDA	ANDA208970	Viona Pharmaceuticals Inc	FELBAMATE	400 mg/1	30 TABLET in 1 BOTTLE (72578-056-06)
72578-056-16	72578-056	HUMAN PRESCRIPTION DRUG	Felbamate	Felbamate	TABLET	ORAL	20200303	N/A	ANDA	ANDA208970	Viona Pharmaceuticals Inc	FELBAMATE	400 mg/1	90 TABLET in 1 BOTTLE (72578-056-16)
72578-056-77	72578-056	HUMAN PRESCRIPTION DRUG	Felbamate	Felbamate	TABLET	ORAL	20200303	N/A	ANDA	ANDA208970	Viona Pharmaceuticals Inc	FELBAMATE	400 mg/1	10 BLISTER PACK in 1 CARTON (72578-056-77) / 10 TABLET in 1 BLISTER PACK (72578-056-30)
70771-1078-1	70771-1078	HUMAN PRESCRIPTION DRUG	Felbamate	Felbamate	TABLET	ORAL	20170815	N/A	ANDA	ANDA208970	Zydus Lifesciences Limited	FELBAMATE	600 mg/1	100 TABLET in 1 BOTTLE (70771-1078-1)
70771-1078-3	70771-1078	HUMAN PRESCRIPTION DRUG	Felbamate	Felbamate	TABLET	ORAL	20170815	N/A	ANDA	ANDA208970	Zydus Lifesciences Limited	FELBAMATE	600 mg/1	30 TABLET in 1 BOTTLE (70771-1078-3)
70771-1078-4	70771-1078	HUMAN PRESCRIPTION DRUG	Felbamate	Felbamate	TABLET	ORAL	20170815	N/A	ANDA	ANDA208970	Zydus Lifesciences Limited	FELBAMATE	600 mg/1	10 BLISTER PACK in 1 CARTON (70771-1078-4) / 10 TABLET in 1 BLISTER PACK
70771-1078-5	70771-1078	HUMAN PRESCRIPTION DRUG	Felbamate	Felbamate	TABLET	ORAL	20170815	N/A	ANDA	ANDA208970	Zydus Lifesciences Limited	FELBAMATE	600 mg/1	500 TABLET in 1 BOTTLE (70771-1078-5)