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
64380-222-01	64380-222	HUMAN PRESCRIPTION DRUG	Omeprazole	omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20240217	N/A	ANDA	ANDA075876	Strides Pharma Science Limited	OMEPRAZOLE	10 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (64380-222-01)
64380-223-01	64380-223	HUMAN PRESCRIPTION DRUG	Omeprazole	omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20240217	N/A	ANDA	ANDA075876	Strides Pharma Science Limited	OMEPRAZOLE	20 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (64380-223-01)
64380-223-02	64380-223	HUMAN PRESCRIPTION DRUG	Omeprazole	omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20240217	N/A	ANDA	ANDA075876	Strides Pharma Science Limited	OMEPRAZOLE	20 mg/1	100 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (64380-223-02)
64380-223-03	64380-223	HUMAN PRESCRIPTION DRUG	Omeprazole	omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20240217	N/A	ANDA	ANDA075876	Strides Pharma Science Limited	OMEPRAZOLE	20 mg/1	1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (64380-223-03)
64380-224-01	64380-224	HUMAN PRESCRIPTION DRUG	Omeprazole	omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20240217	N/A	ANDA	ANDA075876	Strides Pharma Science Limited	OMEPRAZOLE	40 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (64380-224-01)
64380-224-02	64380-224	HUMAN PRESCRIPTION DRUG	Omeprazole	omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20240217	N/A	ANDA	ANDA075876	Strides Pharma Science Limited	OMEPRAZOLE	40 mg/1	500 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (64380-224-02)