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
55319-219-14	55319-219	HUMAN OTC DRUG	Omeprazole	Omeprazole	TABLET, DELAYED RELEASE	ORAL	20250228	N/A	ANDA	ANDA206582	Family Dollar (FAMILY WELLNESS)	OMEPRAZOLE MAGNESIUM	20.6 mg/1	1 BOTTLE, PLASTIC in 1 BOX (55319-219-14) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC
0363-9510-14	0363-9510	HUMAN OTC DRUG	Omeprazole	Omeprazole	TABLET, DELAYED RELEASE	ORAL	20250430	N/A	ANDA	ANDA206582	Walgreens	OMEPRAZOLE MAGNESIUM	20.6 mg/1	1 BOTTLE, PLASTIC in 1 BOX (0363-9510-14) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC
59726-298-14	59726-298	HUMAN OTC DRUG	Omeprazole	Omeprazole	TABLET, DELAYED RELEASE	ORAL	20250131	N/A	ANDA	ANDA206582	P & L Development, LLC	OMEPRAZOLE MAGNESIUM	20.6 mg/1	1 BOTTLE, PLASTIC in 1 BOX (59726-298-14) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC
59726-740-42	59726-740	HUMAN OTC DRUG	Omeprazole	Omeprazole	TABLET, DELAYED RELEASE	ORAL	20250815	N/A	ANDA	ANDA206582	P & L Development, LLC	OMEPRAZOLE MAGNESIUM	20 mg/1	3 BOTTLE, PLASTIC in 1 BOX (59726-740-42) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC
59726-744-42	59726-744	HUMAN OTC DRUG	Omeprazole	Omeprazole	TABLET, DELAYED RELEASE	ORAL	20250829	N/A	ANDA	ANDA206582	P & L Development, LLC	OMEPRAZOLE MAGNESIUM	20 mg/1	3 BOTTLE, PLASTIC in 1 BOX (59726-744-42) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC