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
37835-001-14	37835-001	HUMAN OTC DRUG	Omeprazole	Omeprazole	TABLET, DELAYED RELEASE	ORAL	20190930	N/A	ANDA	ANDA207891	BI-MART	OMEPRAZOLE	20 mg/1	1 BOTTLE in 1 CARTON (37835-001-14) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
37835-001-42	37835-001	HUMAN OTC DRUG	Omeprazole	Omeprazole	TABLET, DELAYED RELEASE	ORAL	20190930	N/A	ANDA	ANDA207891	BI-MART	OMEPRAZOLE	20 mg/1	3 BOTTLE in 1 CARTON (37835-001-42) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
51660-029-14	51660-029	HUMAN OTC DRUG	Omeprazole	Omeprazole	TABLET, DELAYED RELEASE	ORAL	20190601	N/A	ANDA	ANDA207891	OHM LABORATORIES INC.	OMEPRAZOLE	20 mg/1	1 BOTTLE in 1 CARTON (51660-029-14) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
51660-029-27	51660-029	HUMAN OTC DRUG	Omeprazole	Omeprazole	TABLET, DELAYED RELEASE	ORAL	20190601	N/A	ANDA	ANDA207891	OHM LABORATORIES INC.	OMEPRAZOLE	20 mg/1	2 BOTTLE in 1 CARTON (51660-029-27) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
51660-029-44	51660-029	HUMAN OTC DRUG	Omeprazole	Omeprazole	TABLET, DELAYED RELEASE	ORAL	20190601	N/A	ANDA	ANDA207891	OHM LABORATORIES INC.	OMEPRAZOLE	20 mg/1	3 BOTTLE in 1 CARTON (51660-029-44) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
57896-659-42	57896-659	HUMAN OTC DRUG	Omeprazole	Omeprazole	TABLET, DELAYED RELEASE	ORAL	20240523	N/A	ANDA	ANDA207891	GERI-CARE PHARMACEUTICALS, CORP	OMEPRAZOLE	20 mg/1	3 BOTTLE in 1 CARTON (57896-659-42) / 40 TABLET, DELAYED RELEASE in 1 BOTTLE (57896-659-14)