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
71335-9609-5	71335-9609	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20240403	N/A	ANDA	ANDA075757	Bryant Ranch Prepack	OMEPRAZOLE	20 mg/1	20 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-9609-5)
71335-9609-6	71335-9609	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20230428	N/A	ANDA	ANDA075757	Bryant Ranch Prepack	OMEPRAZOLE	20 mg/1	15 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-9609-6)
71335-9609-7	71335-9609	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20221215	N/A	ANDA	ANDA075757	Bryant Ranch Prepack	OMEPRAZOLE	20 mg/1	120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-9609-7)
71335-9609-8	71335-9609	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20240403	N/A	ANDA	ANDA075757	Bryant Ranch Prepack	OMEPRAZOLE	20 mg/1	100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-9609-8)
71335-9609-9	71335-9609	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20240403	N/A	ANDA	ANDA075757	Bryant Ranch Prepack	OMEPRAZOLE	20 mg/1	28 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-9609-9)