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
72578-222-06	72578-222	HUMAN PRESCRIPTION DRUG	prucalopride	prucalopride	TABLET, FILM COATED	ORAL	20260202	N/A	ANDA	ANDA218056	Viona Pharmaceuticals Inc	PRUCALOPRIDE SUCCINATE	2 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (72578-222-06)
72578-221-06	72578-221	HUMAN PRESCRIPTION DRUG	prucalopride	prucalopride	TABLET, FILM COATED	ORAL	20260202	N/A	ANDA	ANDA218056	Viona Pharmaceuticals Inc	PRUCALOPRIDE SUCCINATE	1 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (72578-221-06)
70771-1900-3	70771-1900	HUMAN PRESCRIPTION DRUG	prucalopride	prucalopride	TABLET, FILM COATED	ORAL	20260202	N/A	ANDA	ANDA218056	Zydus Lifesciences Limited	PRUCALOPRIDE SUCCINATE	2 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (70771-1900-3)
70771-1899-3	70771-1899	HUMAN PRESCRIPTION DRUG	prucalopride	prucalopride	TABLET, FILM COATED	ORAL	20260202	N/A	ANDA	ANDA218056	Zydus Lifesciences Limited	PRUCALOPRIDE SUCCINATE	1 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (70771-1899-3)