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
70436-102-09	70436-102	HUMAN PRESCRIPTION DRUG	tetrabenazine	tetrabenazine	TABLET	ORAL	20200302	N/A	ANDA	ANDA213316	Slate Run Pharmaceuticals, LLC	TETRABENAZINE	25 mg/1	112 TABLET in 1 BOTTLE (70436-102-09)
70436-101-09	70436-101	HUMAN PRESCRIPTION DRUG	tetrabenazine	tetrabenazine	TABLET	ORAL	20200302	N/A	ANDA	ANDA213316	Slate Run Pharmaceuticals, LLC	TETRABENAZINE	12.5 mg/1	112 TABLET in 1 BOTTLE (70436-101-09)
23155-939-63	23155-939	HUMAN PRESCRIPTION DRUG	Tetrabenazine	Tetrabenazine	TABLET	ORAL	20250901	N/A	ANDA	ANDA213316	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	TETRABENAZINE	25 mg/1	112 TABLET in 1 BOTTLE (23155-939-63)
23155-938-63	23155-938	HUMAN PRESCRIPTION DRUG	Tetrabenazine	Tetrabenazine	TABLET	ORAL	20250901	N/A	ANDA	ANDA213316	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	TETRABENAZINE	12.5 mg/1	112 TABLET in 1 BOTTLE (23155-938-63)