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
71335-0332-1	71335-0332	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20180716	N/A	ANDA	ANDA075576	Bryant Ranch Prepack	OMEPRAZOLE	20 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0332-1)
71335-0332-2	71335-0332	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20200325	N/A	ANDA	ANDA075576	Bryant Ranch Prepack	OMEPRAZOLE	20 mg/1	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0332-2)
71335-0332-3	71335-0332	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20240528	N/A	ANDA	ANDA075576	Bryant Ranch Prepack	OMEPRAZOLE	20 mg/1	56 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0332-3)
71335-0332-4	71335-0332	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20200508	N/A	ANDA	ANDA075576	Bryant Ranch Prepack	OMEPRAZOLE	20 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0332-4)
71335-0332-5	71335-0332	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20200603	N/A	ANDA	ANDA075576	Bryant Ranch Prepack	OMEPRAZOLE	20 mg/1	20 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0332-5)
71335-0332-6	71335-0332	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20180706	N/A	ANDA	ANDA075576	Bryant Ranch Prepack	OMEPRAZOLE	20 mg/1	15 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0332-6)
71335-0332-7	71335-0332	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20200312	N/A	ANDA	ANDA075576	Bryant Ranch Prepack	OMEPRAZOLE	20 mg/1	120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0332-7)
71335-0332-8	71335-0332	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20240528	N/A	ANDA	ANDA075576	Bryant Ranch Prepack	OMEPRAZOLE	20 mg/1	100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0332-8)
71335-0332-9	71335-0332	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20240528	N/A	ANDA	ANDA075576	Bryant Ranch Prepack	OMEPRAZOLE	20 mg/1	28 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0332-9)
68084-128-01	68084-128	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20091023	20260831	ANDA	ANDA075576	American Health Packaging	OMEPRAZOLE	20 mg/1	100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-128-01) / 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (68084-128-11)
80425-0071-1	80425-0071	HUMAN PRESCRIPTION DRUG	Omeprazole DR	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20191025	N/A	ANDA	ANDA075576	Advanced Rx of Tennessee, LLC	OMEPRAZOLE	20 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0071-1)
80425-0071-2	80425-0071	HUMAN PRESCRIPTION DRUG	Omeprazole DR	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20191025	N/A	ANDA	ANDA075576	Advanced Rx of Tennessee, LLC	OMEPRAZOLE	20 mg/1	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0071-2)
80425-0071-3	80425-0071	HUMAN PRESCRIPTION DRUG	Omeprazole DR	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20191025	N/A	ANDA	ANDA075576	Advanced Rx of Tennessee, LLC	OMEPRAZOLE	20 mg/1	120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0071-3)
82009-022-10	82009-022	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20221115	20280830	ANDA	ANDA075576	Quallent Pharmaceuticals Health LLC	OMEPRAZOLE	20 mg/1	1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (82009-022-10)