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
16714-715-02	16714-715	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20191025	N/A	ANDA	ANDA075576	NorthStar Rx LLC	OMEPRAZOLE	20 mg/1	100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (16714-715-02)
16714-715-03	16714-715	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20191025	N/A	ANDA	ANDA075576	NorthStar Rx LLC	OMEPRAZOLE	20 mg/1	1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (16714-715-03)
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)
80425-0415-1	80425-0415	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20240715	N/A	ANDA	ANDA075576	Advanced Rx of Tennessee, LLC	OMEPRAZOLE	20 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0415-1)
80425-0415-2	80425-0415	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20240715	N/A	ANDA	ANDA075576	Advanced Rx of Tennessee, LLC	OMEPRAZOLE	20 mg/1	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0415-2)
80425-0415-3	80425-0415	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20240715	N/A	ANDA	ANDA075576	Advanced Rx of Tennessee, LLC	OMEPRAZOLE	20 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0415-3)
80425-0415-4	80425-0415	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20240715	N/A	ANDA	ANDA075576	Advanced Rx of Tennessee, LLC	OMEPRAZOLE	20 mg/1	120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0415-4)
63187-805-60	63187-805	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20170102	N/A	ANDA	ANDA075576	Proficient Rx LP	OMEPRAZOLE	10 mg/1	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (63187-805-60)
63187-805-90	63187-805	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20170102	N/A	ANDA	ANDA075576	Proficient Rx LP	OMEPRAZOLE	10 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (63187-805-90)
51655-061-25	51655-061	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20200601	N/A	ANDA	ANDA075576	Northwind Health Company, LLC	OMEPRAZOLE	20 mg/1	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (51655-061-25)
51655-061-26	51655-061	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20240125	N/A	ANDA	ANDA075576	Northwind Health Company, LLC	OMEPRAZOLE	20 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (51655-061-26)
51655-061-52	51655-061	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20200601	N/A	ANDA	ANDA075576	Northwind Health Company, LLC	OMEPRAZOLE	20 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (51655-061-52)