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
50228-438-05	50228-438	HUMAN PRESCRIPTION DRUG	Naproxen and esomeprazole magnesium	Naproxen and esomeprazole magnesium	TABLET, DELAYED RELEASE	ORAL	20231011	N/A	ANDA	ANDA217738	ScieGen Pharmaceuticals, Inc	ESOMEPRAZOLE MAGNESIUM; NAPROXEN	20 mg/1; 500 mg/1	500 TABLET, DELAYED RELEASE in 1 BOTTLE (50228-438-05)
50228-438-30	50228-438	HUMAN PRESCRIPTION DRUG	Naproxen and esomeprazole magnesium	Naproxen and esomeprazole magnesium	TABLET, DELAYED RELEASE	ORAL	20231011	N/A	ANDA	ANDA217738	ScieGen Pharmaceuticals, Inc	ESOMEPRAZOLE MAGNESIUM; NAPROXEN	20 mg/1; 500 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (50228-438-30)
50228-438-60	50228-438	HUMAN PRESCRIPTION DRUG	Naproxen and esomeprazole magnesium	Naproxen and esomeprazole magnesium	TABLET, DELAYED RELEASE	ORAL	20240312	N/A	ANDA	ANDA217738	ScieGen Pharmaceuticals, Inc	ESOMEPRAZOLE MAGNESIUM; NAPROXEN	20 mg/1; 500 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (50228-438-60)
50228-437-60	50228-437	HUMAN PRESCRIPTION DRUG	Naproxen and esomeprazole magnesium	Naproxen and esomeprazole magnesium	TABLET, DELAYED RELEASE	ORAL	20240312	N/A	ANDA	ANDA217738	ScieGen Pharmaceuticals, Inc	ESOMEPRAZOLE MAGNESIUM; NAPROXEN	20 mg/1; 375 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (50228-437-60)
50228-437-30	50228-437	HUMAN PRESCRIPTION DRUG	Naproxen and esomeprazole magnesium	Naproxen and esomeprazole magnesium	TABLET, DELAYED RELEASE	ORAL	20231011	N/A	ANDA	ANDA217738	ScieGen Pharmaceuticals, Inc	ESOMEPRAZOLE MAGNESIUM; NAPROXEN	20 mg/1; 375 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (50228-437-30)
50228-437-10	50228-437	HUMAN PRESCRIPTION DRUG	Naproxen and esomeprazole magnesium	Naproxen and esomeprazole magnesium	TABLET, DELAYED RELEASE	ORAL	20231011	N/A	ANDA	ANDA217738	ScieGen Pharmaceuticals, Inc	ESOMEPRAZOLE MAGNESIUM; NAPROXEN	20 mg/1; 375 mg/1	1000 TABLET, DELAYED RELEASE in 1 BOTTLE (50228-437-10)