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
71335-9744-2	71335-9744	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20230710	N/A	ANDA	ANDA091352	Bryant Ranch Prepack	OMEPRAZOLE	40 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-9744-2)
71335-9744-3	71335-9744	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20230710	N/A	ANDA	ANDA091352	Bryant Ranch Prepack	OMEPRAZOLE	40 mg/1	20 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-9744-3)
71335-9744-4	71335-9744	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20230710	N/A	ANDA	ANDA091352	Bryant Ranch Prepack	OMEPRAZOLE	40 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-9744-4)
71335-9744-5	71335-9744	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20230710	N/A	ANDA	ANDA091352	Bryant Ranch Prepack	OMEPRAZOLE	40 mg/1	14 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-9744-5)
71335-9744-6	71335-9744	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20230710	N/A	ANDA	ANDA091352	Bryant Ranch Prepack	OMEPRAZOLE	40 mg/1	120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-9744-6)
71335-9744-7	71335-9744	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20230710	N/A	ANDA	ANDA091352	Bryant Ranch Prepack	OMEPRAZOLE	40 mg/1	100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-9744-7)
71335-9744-8	71335-9744	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20230710	N/A	ANDA	ANDA091352	Bryant Ranch Prepack	OMEPRAZOLE	40 mg/1	180 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-9744-8)
65841-759-05	65841-759	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20121123	N/A	ANDA	ANDA091352	Zydus Lifesciences Limited	OMEPRAZOLE	10 mg/1	500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65841-759-05)
65841-759-06	65841-759	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20121123	N/A	ANDA	ANDA091352	Zydus Lifesciences Limited	OMEPRAZOLE	10 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65841-759-06)
65841-759-01	65841-759	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20121123	N/A	ANDA	ANDA091352	Zydus Lifesciences Limited	OMEPRAZOLE	10 mg/1	100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65841-759-01)