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
72865-231-60	72865-231	HUMAN PRESCRIPTION DRUG	Maraviroc	Maraviroc	TABLET, FILM COATED	ORAL	20230601	N/A	ANDA	ANDA203347	XLCare Pharmaceuticals Inc.	MARAVIROC	150 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (72865-231-60)
31722-579-60	31722-579	HUMAN PRESCRIPTION DRUG	Maraviroc	Maraviroc	TABLET, FILM COATED	ORAL	20220206	N/A	ANDA	ANDA203347	Camber Pharmaceuticals, Inc.	MARAVIROC	150 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (31722-579-60)
72865-232-60	72865-232	HUMAN PRESCRIPTION DRUG	Maraviroc	Maraviroc	TABLET, FILM COATED	ORAL	20230601	N/A	ANDA	ANDA203347	XLCare Pharmaceuticals Inc.	MARAVIROC	300 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (72865-232-60)
31722-580-60	31722-580	HUMAN PRESCRIPTION DRUG	Maraviroc	Maraviroc	TABLET, FILM COATED	ORAL	20220206	N/A	ANDA	ANDA203347	Camber Pharmaceuticals, Inc.	MARAVIROC	300 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (31722-580-60)
68554-3079-0	68554-3079	HUMAN PRESCRIPTION DRUG	Maraviroc	Maraviroc	TABLET, FILM COATED	ORAL	20220206	N/A	ANDA	ANDA203347	Hetero Labs Limited	MARAVIROC	150 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (68554-3079-0)
68554-3080-0	68554-3080	HUMAN PRESCRIPTION DRUG	Maraviroc	Maraviroc	TABLET, FILM COATED	ORAL	20220206	N/A	ANDA	ANDA203347	Hetero Labs Limited	MARAVIROC	300 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (68554-3080-0)