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
65862-622-99	65862-622	HUMAN PRESCRIPTION DRUG	Flecainide Acetate	Flecainide Acetate	TABLET	ORAL	20171103	N/A	ANDA	ANDA202821	Aurobindo Pharma Limited	FLECAINIDE ACETATE	100 mg/1	1000 TABLET in 1 BOTTLE (65862-622-99)
57237-065-01	57237-065	HUMAN PRESCRIPTION DRUG	Flecainide Acetate	Flecainide Acetate	TABLET	ORAL	20150708	N/A	ANDA	ANDA202821	Rising Pharma Holdings, Inc.	FLECAINIDE ACETATE	150 mg/1	100 TABLET in 1 BOTTLE (57237-065-01)
65862-621-01	65862-621	HUMAN PRESCRIPTION DRUG	Flecainide Acetate	Flecainide Acetate	TABLET	ORAL	20171103	N/A	ANDA	ANDA202821	Aurobindo Pharma Limited	FLECAINIDE ACETATE	50 mg/1	100 TABLET in 1 BOTTLE (65862-621-01)
65862-621-30	65862-621	HUMAN PRESCRIPTION DRUG	Flecainide Acetate	Flecainide Acetate	TABLET	ORAL	20171103	N/A	ANDA	ANDA202821	Aurobindo Pharma Limited	FLECAINIDE ACETATE	50 mg/1	30 TABLET in 1 BOTTLE (65862-621-30)
65862-621-99	65862-621	HUMAN PRESCRIPTION DRUG	Flecainide Acetate	Flecainide Acetate	TABLET	ORAL	20171103	N/A	ANDA	ANDA202821	Aurobindo Pharma Limited	FLECAINIDE ACETATE	50 mg/1	1000 TABLET in 1 BOTTLE (65862-621-99)
57237-064-01	57237-064	HUMAN PRESCRIPTION DRUG	Flecainide Acetate	Flecainide Acetate	TABLET	ORAL	20150708	N/A	ANDA	ANDA202821	Rising Pharma Holdings, Inc.	FLECAINIDE ACETATE	100 mg/1	100 TABLET in 1 BOTTLE (57237-064-01)