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
43598-286-52	43598-286	HUMAN OTC DRUG	Omeprazole	Omeprazole	TABLET, DELAYED RELEASE	ORAL	20181106	N/A	ANDA	ANDA207740	Dr. Reddys Laboratories Inc	OMEPRAZOLE	20 mg/1	14 TABLET, DELAYED RELEASE in 1 BOTTLE (43598-286-52)
43598-286-74	43598-286	HUMAN OTC DRUG	Omeprazole	Omeprazole	TABLET, DELAYED RELEASE	ORAL	20181106	N/A	ANDA	ANDA207740	Dr. Reddys Laboratories Inc	OMEPRAZOLE	20 mg/1	1 BLISTER PACK in 1 CARTON (43598-286-74) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK
43598-286-25	43598-286	HUMAN OTC DRUG	Omeprazole	Omeprazole	TABLET, DELAYED RELEASE	ORAL	20181106	N/A	ANDA	ANDA207740	Dr. Reddys Laboratories Inc	OMEPRAZOLE	20 mg/1	2 BLISTER PACK in 1 CARTON (43598-286-25) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK
43598-286-33	43598-286	HUMAN OTC DRUG	Omeprazole	Omeprazole	TABLET, DELAYED RELEASE	ORAL	20181106	N/A	ANDA	ANDA207740	Dr. Reddys Laboratories Inc	OMEPRAZOLE	20 mg/1	3 BOTTLE in 1 CARTON (43598-286-33) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE (43598-286-52)
43598-286-27	43598-286	HUMAN OTC DRUG	Omeprazole	Omeprazole	TABLET, DELAYED RELEASE	ORAL	20181106	N/A	ANDA	ANDA207740	Dr. Reddys Laboratories Inc	OMEPRAZOLE	20 mg/1	2 BOTTLE in 1 CARTON (43598-286-27) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE (43598-286-52)
79903-305-28	79903-305	HUMAN OTC DRUG	Omeprazole	Omeprazole	TABLET, DELAYED RELEASE	ORAL	20250203	N/A	ANDA	ANDA207740	Walmart Inc.	OMEPRAZOLE	20 mg/1	2 BOTTLE in 1 CARTON (79903-305-28) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE (79903-305-14)