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
63868-471-14	63868-471	HUMAN OTC DRUG	Omeprazole	Omeprazole	TABLET, DELAYED RELEASE	ORAL	20200201	N/A	ANDA	ANDA207740	Chain Drug Marketing Association INC	OMEPRAZOLE	20 mg/1	1 BOTTLE in 1 CARTON (63868-471-14) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
63868-471-42	63868-471	HUMAN OTC DRUG	Omeprazole	Omeprazole	TABLET, DELAYED RELEASE	ORAL	20200201	N/A	ANDA	ANDA207740	Chain Drug Marketing Association INC	OMEPRAZOLE	20 mg/1	3 BOTTLE in 1 CARTON (63868-471-42) / 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)
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
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
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)
46122-739-03	46122-739	HUMAN OTC DRUG	Omeprazole	Omeprazole	TABLET, DELAYED RELEASE	ORAL	20230830	N/A	ANDA	ANDA207740	AMERISOURCEBERGEN DRUG CORPORATION	OMEPRAZOLE	20 mg/1	2 BOTTLE in 1 CARTON (46122-739-03) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
46122-739-04	46122-739	HUMAN OTC DRUG	Omeprazole	Omeprazole	TABLET, DELAYED RELEASE	ORAL	20230830	N/A	ANDA	ANDA207740	AMERISOURCEBERGEN DRUG CORPORATION	OMEPRAZOLE	20 mg/1	3 BOTTLE in 1 CARTON (46122-739-04) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
46122-739-74	46122-739	HUMAN OTC DRUG	Omeprazole	Omeprazole	TABLET, DELAYED RELEASE	ORAL	20230830	N/A	ANDA	ANDA207740	AMERISOURCEBERGEN DRUG CORPORATION	OMEPRAZOLE	20 mg/1	1 BOTTLE in 1 CARTON (46122-739-74) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
68001-441-39	68001-441	HUMAN OTC DRUG	Omeprazole	Omeprazole	TABLET, DELAYED RELEASE	ORAL	20200619	N/A	ANDA	ANDA207740	BluePoint Laboratories	OMEPRAZOLE	20 mg/1	2 BOTTLE in 1 CARTON (68001-441-39) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE (68001-441-55)
68001-441-40	68001-441	HUMAN OTC DRUG	Omeprazole	Omeprazole	TABLET, DELAYED RELEASE	ORAL	20200619	N/A	ANDA	ANDA207740	BluePoint Laboratories	OMEPRAZOLE	20 mg/1	3 BOTTLE in 1 CARTON (68001-441-40) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE (68001-441-55)
68001-441-98	68001-441	HUMAN OTC DRUG	Omeprazole	Omeprazole	TABLET, DELAYED RELEASE	ORAL	20200619	N/A	ANDA	ANDA207740	BluePoint Laboratories	OMEPRAZOLE	20 mg/1	1 BOTTLE in 1 CARTON (68001-441-98) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE (68001-441-55)
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
43598-286-27	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)
43598-286-32	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 (43598-286-32) / 7 TABLET, DELAYED RELEASE in 1 BLISTER PACK (43598-286-70)