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
31722-527-01	31722-527	HUMAN PRESCRIPTION DRUG	omeprazole	omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20190926	N/A	ANDA	ANDA204012	Camber Pharmaceuticals, Inc.	OMEPRAZOLE	10 mg/1	100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (31722-527-01)
31722-527-30	31722-527	HUMAN PRESCRIPTION DRUG	omeprazole	omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20190926	N/A	ANDA	ANDA204012	Camber Pharmaceuticals, Inc.	OMEPRAZOLE	10 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (31722-527-30)
31722-528-01	31722-528	HUMAN PRESCRIPTION DRUG	omeprazole	omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20190926	N/A	ANDA	ANDA204012	Camber Pharmaceuticals, Inc.	OMEPRAZOLE	20 mg/1	100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (31722-528-01)
31722-528-30	31722-528	HUMAN PRESCRIPTION DRUG	omeprazole	omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20190926	N/A	ANDA	ANDA204012	Camber Pharmaceuticals, Inc.	OMEPRAZOLE	20 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (31722-528-30)