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
43598-841-52	43598-841	HUMAN OTC DRUG	Omeprazole	Omeprazole	TABLET, DELAYED RELEASE	ORAL	20201001	N/A	ANDA	ANDA207740	Dr. Reddys Laboratories Inc	OMEPRAZOLE	20 mg/1	1 BOTTLE in 1 CARTON (43598-841-52) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
83324-141-14	83324-141	HUMAN OTC DRUG	Omeprazole	Omeprazole	TABLET, DELAYED RELEASE	ORAL	20250401	N/A	ANDA	ANDA207740	Chain Drug Marketing Association INC	OMEPRAZOLE	20 mg/1	1 BOTTLE in 1 CARTON (83324-141-14) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
83324-141-42	83324-141	HUMAN OTC DRUG	Omeprazole	Omeprazole	TABLET, DELAYED RELEASE	ORAL	20250401	N/A	ANDA	ANDA207740	Chain Drug Marketing Association INC	OMEPRAZOLE	20 mg/1	3 BOTTLE in 1 CARTON (83324-141-42) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
0363-1607-14	0363-1607	HUMAN OTC DRUG	Omeprazole	Omeprazole	TABLET, DELAYED RELEASE	ORAL	20200115	N/A	ANDA	ANDA207740	Walgreens Company	OMEPRAZOLE	20 mg/1	14 TABLET, DELAYED RELEASE in 1 BOTTLE (0363-1607-14)
0363-1607-28	0363-1607	HUMAN OTC DRUG	Omeprazole	Omeprazole	TABLET, DELAYED RELEASE	ORAL	20200115	N/A	ANDA	ANDA207740	Walgreens Company	OMEPRAZOLE	20 mg/1	2 BOTTLE in 1 CARTON (0363-1607-28) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE (0363-1607-14)
0363-1607-42	0363-1607	HUMAN OTC DRUG	Omeprazole	Omeprazole	TABLET, DELAYED RELEASE	ORAL	20200115	N/A	ANDA	ANDA207740	Walgreens Company	OMEPRAZOLE	20 mg/1	3 BOTTLE in 1 CARTON (0363-1607-42) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE (0363-1607-14)