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
43598-841-42	43598-841	HUMAN OTC DRUG	Omeprazole	Omeprazole	TABLET, DELAYED RELEASE	ORAL	20201001	N/A	ANDA	ANDA207740	Dr. Reddys Laboratories Inc	OMEPRAZOLE	20 mg/1	3 BOTTLE in 1 CARTON (43598-841-42) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
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
71713-201-01	71713-201	HUMAN OTC DRUG	Omeprazole	Omeprazole	TABLET, DELAYED RELEASE	ORAL	20190531	N/A	ANDA	ANDA207740	Thirty Madison Inc	OMEPRAZOLE	20 mg/1	1 BOTTLE in 1 CARTON (71713-201-01) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
71713-201-03	71713-201	HUMAN OTC DRUG	Omeprazole	Omeprazole	TABLET, DELAYED RELEASE	ORAL	20190531	N/A	ANDA	ANDA207740	Thirty Madison Inc	OMEPRAZOLE	20 mg/1	3 BOTTLE in 1 CARTON (71713-201-03) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
21130-018-14	21130-018	HUMAN OTC DRUG	Omeprazole	Omeprazole	TABLET, DELAYED RELEASE	ORAL	20230915	N/A	ANDA	ANDA207740	Albertsons Companies	OMEPRAZOLE	20 mg/1	1 BOTTLE in 1 CARTON (21130-018-14) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
21130-018-28	21130-018	HUMAN OTC DRUG	Omeprazole	Omeprazole	TABLET, DELAYED RELEASE	ORAL	20230915	N/A	ANDA	ANDA207740	Albertsons Companies	OMEPRAZOLE	20 mg/1	2 BOTTLE in 1 CARTON (21130-018-28) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
21130-018-42	21130-018	HUMAN OTC DRUG	Omeprazole	Omeprazole	TABLET, DELAYED RELEASE	ORAL	20230915	N/A	ANDA	ANDA207740	Albertsons Companies	OMEPRAZOLE	20 mg/1	3 BOTTLE in 1 CARTON (21130-018-42) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
57896-960-42	57896-960	HUMAN OTC DRUG	Omeprazole	Omeprazole	TABLET, DELAYED RELEASE	ORAL	20181106	N/A	ANDA	ANDA207740	GERICARE PHARMACEUTICALS	OMEPRAZOLE	20 mg/1	3 BOTTLE in 1 CARTON (57896-960-42) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE (57896-960-14)