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
51525-0430-1	51525-0430	HUMAN PRESCRIPTION DRUG	Felbamate	felbamate	TABLET	ORAL	20111111	N/A	NDA AUTHORIZED GENERIC	NDA020189	Wallace Pharmaceuticals Inc.	FELBAMATE	400 mg/1	100 TABLET in 1 BOTTLE (51525-0430-1)
51525-0431-1	51525-0431	HUMAN PRESCRIPTION DRUG	Felbamate	felbamate	TABLET	ORAL	20111111	N/A	NDA AUTHORIZED GENERIC	NDA020189	Wallace Pharmaceuticals Inc.	FELBAMATE	600 mg/1	100 TABLET in 1 BOTTLE (51525-0431-1)
51525-0442-3	51525-0442	HUMAN PRESCRIPTION DRUG	Felbamate	felbamate	SUSPENSION	ORAL	20111123	N/A	NDA AUTHORIZED GENERIC	NDA020189	Wallace Pharmaceuticals Inc.	FELBAMATE	600 mg/5mL	946 mL in 1 BOTTLE (51525-0442-3)
51525-0442-8	51525-0442	HUMAN PRESCRIPTION DRUG	Felbamate	felbamate	SUSPENSION	ORAL	20111123	N/A	NDA AUTHORIZED GENERIC	NDA020189	Wallace Pharmaceuticals Inc.	FELBAMATE	600 mg/5mL	237 mL in 1 BOTTLE (51525-0442-8)
0037-0430-01	0037-0430	HUMAN PRESCRIPTION DRUG	Felbatol	felbamate	TABLET	ORAL	19930729	N/A	NDA	NDA020189	Meda Pharmaceuticals Inc.	FELBAMATE	400 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (0037-0430-01)
0037-0431-01	0037-0431	HUMAN PRESCRIPTION DRUG	Felbatol	felbamate	TABLET	ORAL	19930729	N/A	NDA	NDA020189	Meda Pharmaceuticals Inc.	FELBAMATE	600 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (0037-0431-01)
0037-0442-17	0037-0442	HUMAN PRESCRIPTION DRUG	Felbatol	felbamate	SUSPENSION	ORAL	19930729	20260331	NDA	NDA020189	Meda Pharmaceuticals Inc.	FELBAMATE	600 mg/5mL	946 mL in 1 BOTTLE, PLASTIC (0037-0442-17)
0037-0442-67	0037-0442	HUMAN PRESCRIPTION DRUG	Felbatol	felbamate	SUSPENSION	ORAL	19930729	20251130	NDA	NDA020189	Meda Pharmaceuticals Inc.	FELBAMATE	600 mg/5mL	237 mL in 1 BOTTLE, PLASTIC (0037-0442-67)