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
72319-024-02	72319-024	HUMAN PRESCRIPTION DRUG	Maraviroc	Maraviroc	TABLET, FILM COATED	ORAL	20230915	N/A	ANDA	ANDA217114	i3 Pharmaceuticals, LLC	MARAVIROC	150 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (72319-024-02)
72319-025-02	72319-025	HUMAN PRESCRIPTION DRUG	Maraviroc	Maraviroc	TABLET, FILM COATED	ORAL	20230915	N/A	ANDA	ANDA217114	i3 Pharmaceuticals, LLC	MARAVIROC	300 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (72319-025-02)
73141-025-02	73141-025	HUMAN PRESCRIPTION DRUG	Maraviroc	Maraviroc	TABLET, FILM COATED	ORAL	20240516	N/A	ANDA	ANDA217114	A2A Integrated Pharmaceuticals	MARAVIROC	300 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (73141-025-02)
73141-024-02	73141-024	HUMAN PRESCRIPTION DRUG	Maraviroc	Maraviroc	TABLET, FILM COATED	ORAL	20240516	N/A	ANDA	ANDA217114	A2A Integrated Pharmaceuticals	MARAVIROC	150 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (73141-024-02)