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
53002-9850-1	53002-9850	HUMAN PRESCRIPTION DRUG	Mupirocin	Mupirocin	OINTMENT	TOPICAL	20171001	N/A	ANDA	ANDA090480	RPK Pharmaceuticals, Inc.	MUPIROCIN	20 mg/g	22 g in 1 TUBE (53002-9850-1)
68788-8534-2	68788-8534	HUMAN PRESCRIPTION DRUG	Mupirocin	Mupirocin	OINTMENT	TOPICAL	20231023	N/A	ANDA	ANDA090480	Preferred Pharmaceuticals Inc.	MUPIROCIN	20 mg/g	22 g in 1 TUBE (68788-8534-2)
63187-015-22	63187-015	HUMAN PRESCRIPTION DRUG	Mupirocin	Mupirocin	OINTMENT	TOPICAL	20181101	N/A	ANDA	ANDA090480	Proficient Rx LP	MUPIROCIN	20 mg/g	22 g in 1 TUBE (63187-015-22)
68071-4111-2	68071-4111	HUMAN PRESCRIPTION DRUG	Mupirocin	Mupirocin	OINTMENT	TOPICAL	20171004	N/A	ANDA	ANDA090480	NuCare Pharmaceuticals,Inc.	MUPIROCIN	20 mg/g	22 g in 1 BOX (68071-4111-2)
81033-020-50	81033-020	HUMAN PRESCRIPTION DRUG	Mupirocin	Mupirocin	OINTMENT	TOPICAL	20211015	N/A	ANDA	ANDA090480	Kesin Pharma Corporation	MUPIROCIN	20 mg/g	50 TUBE in 1 PACKAGE (81033-020-50) / 1 g in 1 TUBE (81033-020-01)
81033-020-99	81033-020	HUMAN PRESCRIPTION DRUG	Mupirocin	Mupirocin	OINTMENT	TOPICAL	20211015	N/A	ANDA	ANDA090480	Kesin Pharma Corporation	MUPIROCIN	20 mg/g	100 TUBE in 1 PACKAGE (81033-020-99) / 1 g in 1 TUBE (81033-020-01)
68462-180-22	68462-180	HUMAN PRESCRIPTION DRUG	Mupirocin	Mupirocin	OINTMENT	TOPICAL	20110608	N/A	ANDA	ANDA090480	Glenmark Pharmaceuticals Inc., USA	MUPIROCIN	20 mg/g	22 g in 1 TUBE (68462-180-22)