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
75987-030-73	75987-030	HUMAN PRESCRIPTION DRUG	Vimovo	Naproxen and Esomeprazole Magnesium	TABLET, DELAYED RELEASE	ORAL	20100706	N/A	NDA	NDA022511	Horizon Therapeutics USA, Inc.	ESOMEPRAZOLE MAGNESIUM; NAPROXEN	20 mg/1; 500 mg/1	1 BOTTLE in 1 CARTON (75987-030-73) / 6 TABLET, DELAYED RELEASE in 1 BOTTLE
75987-031-04	75987-031	HUMAN PRESCRIPTION DRUG	Vimovo	Naproxen and Esomeprazole Magnesium	TABLET, DELAYED RELEASE	ORAL	20100706	N/A	NDA	NDA022511	Horizon Therapeutics USA, Inc.	ESOMEPRAZOLE MAGNESIUM; NAPROXEN	20 mg/1; 375 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (75987-031-04)
70748-215-07	70748-215	HUMAN PRESCRIPTION DRUG	NAPROXEN AND ESOMEPRAZOLE MAGNESIUM	NAPROXEN AND ESOMEPRAZOLE MAGNESIUM	TABLET, DELAYED RELEASE	ORAL	20200304	20240930	NDA AUTHORIZED GENERIC	NDA022511	Lupin Pharmaceuticals, Inc.	ESOMEPRAZOLE MAGNESIUM; NAPROXEN	20 mg/1; 375 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (70748-215-07)
70748-216-07	70748-216	HUMAN PRESCRIPTION DRUG	NAPROXEN AND ESOMEPRAZOLE MAGNESIUM	NAPROXEN AND ESOMEPRAZOLE MAGNESIUM	TABLET, DELAYED RELEASE	ORAL	20200304	20240930	NDA AUTHORIZED GENERIC	NDA022511	Lupin Pharmaceuticals, Inc.	ESOMEPRAZOLE MAGNESIUM; NAPROXEN	20 mg/1; 500 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (70748-216-07)
75987-030-04	75987-030	HUMAN PRESCRIPTION DRUG	Vimovo	Naproxen and Esomeprazole Magnesium	TABLET, DELAYED RELEASE	ORAL	20100706	N/A	NDA	NDA022511	Horizon Therapeutics USA, Inc.	ESOMEPRAZOLE MAGNESIUM; NAPROXEN	20 mg/1; 500 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (75987-030-04)