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
51655-893-83	51655-893	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20240215	N/A	ANDA	ANDA075757	Northwind Pharmaceuticals, LLC	OMEPRAZOLE	20 mg/1	180 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (51655-893-83)
51655-893-84	51655-893	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20220919	N/A	ANDA	ANDA075757	Northwind Pharmaceuticals, LLC	OMEPRAZOLE	20 mg/1	14 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (51655-893-84)
71335-9609-0	71335-9609	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20240403	N/A	ANDA	ANDA075757	Bryant Ranch Prepack	OMEPRAZOLE	20 mg/1	7 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-9609-0)
71335-9609-1	71335-9609	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20230125	N/A	ANDA	ANDA075757	Bryant Ranch Prepack	OMEPRAZOLE	20 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-9609-1)
71335-9609-2	71335-9609	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20221229	N/A	ANDA	ANDA075757	Bryant Ranch Prepack	OMEPRAZOLE	20 mg/1	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-9609-2)