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
70771-1531-6	70771-1531	HUMAN PRESCRIPTION DRUG	dimethyl fumarate	dimethyl fumarate	CAPSULE, DELAYED RELEASE	ORAL	20200928	N/A	ANDA	ANDA210538	Zydus Lifesciences Limited	DIMETHYL FUMARATE	240 mg/1	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70771-1531-6)
70771-1531-8	70771-1531	HUMAN PRESCRIPTION DRUG	dimethyl fumarate	dimethyl fumarate	CAPSULE, DELAYED RELEASE	ORAL	20200928	N/A	ANDA	ANDA210538	Zydus Lifesciences Limited	DIMETHYL FUMARATE	240 mg/1	46 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70771-1531-8)
70771-1530-7	70771-1530	HUMAN PRESCRIPTION DRUG	dimethyl fumarate	dimethyl fumarate	CAPSULE, DELAYED RELEASE	ORAL	20200928	N/A	ANDA	ANDA210538	Zydus Lifesciences Limited	DIMETHYL FUMARATE	120 mg/1	14 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70771-1530-7)
70710-1205-8	70710-1205	HUMAN PRESCRIPTION DRUG	dimethyl fumarate	dimethyl fumarate	CAPSULE, DELAYED RELEASE	ORAL	20200928	N/A	ANDA	ANDA210538	Zydus Pharmaceuticals USA Inc.	DIMETHYL FUMARATE	240 mg/1	46 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70710-1205-8)
70710-1205-6	70710-1205	HUMAN PRESCRIPTION DRUG	dimethyl fumarate	dimethyl fumarate	CAPSULE, DELAYED RELEASE	ORAL	20200928	N/A	ANDA	ANDA210538	Zydus Pharmaceuticals USA Inc.	DIMETHYL FUMARATE	240 mg/1	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70710-1205-6)
70710-1204-7	70710-1204	HUMAN PRESCRIPTION DRUG	dimethyl fumarate	dimethyl fumarate	CAPSULE, DELAYED RELEASE	ORAL	20200928	N/A	ANDA	ANDA210538	Zydus Pharmaceuticals USA Inc.	DIMETHYL FUMARATE	120 mg/1	14 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70710-1204-7)