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
0093-6450-56	0093-6450	HUMAN PRESCRIPTION DRUG	Esomeprazole Magnesium	Esomeprazole Magnesium	CAPSULE, DELAYED RELEASE	ORAL	20150217	20241031	ANDA	ANDA078003	Teva Pharmaceuticals USA, Inc.	ESOMEPRAZOLE MAGNESIUM DIHYDRATE	20 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0093-6450-56)
0093-6450-98	0093-6450	HUMAN PRESCRIPTION DRUG	Esomeprazole Magnesium	Esomeprazole Magnesium	CAPSULE, DELAYED RELEASE	ORAL	20150217	20241031	ANDA	ANDA078003	Teva Pharmaceuticals USA, Inc.	ESOMEPRAZOLE MAGNESIUM DIHYDRATE	20 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0093-6450-98)
0093-6451-56	0093-6451	HUMAN PRESCRIPTION DRUG	Esomeprazole Magnesium	Esomeprazole Magnesium	CAPSULE, DELAYED RELEASE	ORAL	20150217	20250131	ANDA	ANDA078003	Teva Pharmaceuticals USA, Inc.	ESOMEPRAZOLE MAGNESIUM DIHYDRATE	40 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0093-6451-56)
0093-6451-98	0093-6451	HUMAN PRESCRIPTION DRUG	Esomeprazole Magnesium	Esomeprazole Magnesium	CAPSULE, DELAYED RELEASE	ORAL	20150217	20250131	ANDA	ANDA078003	Teva Pharmaceuticals USA, Inc.	ESOMEPRAZOLE MAGNESIUM DIHYDRATE	40 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0093-6451-98)
61919-243-30	61919-243	HUMAN PRESCRIPTION DRUG	ESOMEPRAZOLE MAGNESIUM	ESOMEPRAZOLE MAGNESIUM	CAPSULE, DELAYED RELEASE	ORAL	20210224	N/A	ANDA	ANDA078003	DIRECT RX	ESOMEPRAZOLE MAGNESIUM DIHYDRATE	40 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (61919-243-30)