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
72485-415-04	72485-415	HUMAN PRESCRIPTION DRUG	mycophenolate mofetil	mycophenolate mofetil	INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION	INTRAVENOUS	20230706	N/A	ANDA	ANDA216390	ARMAS PHARMACEUTICALS INC	MYCOPHENOLATE MOFETIL	500 mg/20mL	4 VIAL in 1 CARTON (72485-415-04) / 20 mL in 1 VIAL
81293-000-04	81293-000	HUMAN PRESCRIPTION DRUG	mycophenolate mofetil	mycophenolate mofetil	INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION	INTRAVENOUS	20230430	N/A	ANDA	ANDA216390	Steriscience Pte. Limited	MYCOPHENOLATE MOFETIL	500 mg/20mL	4 VIAL in 1 CARTON (81293-000-04) / 20 mL in 1 VIAL
83270-000-04	83270-000	HUMAN PRESCRIPTION DRUG	mycophenolate mofetil	mycophenolate mofetil	INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION	INTRAVENOUS	20230430	N/A	ANDA	ANDA216390	STELIS BIOPHARMA LIMITED	MYCOPHENOLATE MOFETIL	500 mg/20mL	4 VIAL in 1 CARTON (83270-000-04) / 20 mL in 1 VIAL