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
63187-070-72	63187-070	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20181101	N/A	ANDA	ANDA076048	Proficient Rx LP	OMEPRAZOLE	20 mg/1	120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (63187-070-72)
63187-070-78	63187-070	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20181101	N/A	ANDA	ANDA076048	Proficient Rx LP	OMEPRAZOLE	20 mg/1	180 CAPSULE, DELAYED RELEASE in 1 BOTTLE (63187-070-78)
63187-070-90	63187-070	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20181101	N/A	ANDA	ANDA076048	Proficient Rx LP	OMEPRAZOLE	20 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (63187-070-90)
63187-170-30	63187-170	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20190101	N/A	ANDA	ANDA076048	Proficient Rx LP	OMEPRAZOLE	40 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (63187-170-30)
63187-170-60	63187-170	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20190101	N/A	ANDA	ANDA076048	Proficient Rx LP	OMEPRAZOLE	40 mg/1	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (63187-170-60)
63187-170-90	63187-170	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20190101	N/A	ANDA	ANDA076048	Proficient Rx LP	OMEPRAZOLE	40 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (63187-170-90)
60505-0065-0	60505-0065	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20031111	20260331	ANDA	ANDA076048	Apotex Corp	OMEPRAZOLE	20 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (60505-0065-0)
60505-0065-1	60505-0065	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20031111	20270131	ANDA	ANDA076048	Apotex Corp	OMEPRAZOLE	20 mg/1	1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (60505-0065-1)
60505-0065-2	60505-0065	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20031111	20270131	ANDA	ANDA076048	Apotex Corp	OMEPRAZOLE	20 mg/1	100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (60505-0065-2)
60505-0145-0	60505-0145	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20031111	20260331	ANDA	ANDA076048	Apotex Corp	OMEPRAZOLE	10 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (60505-0145-0)
60505-0145-2	60505-0145	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20031111	20270131	ANDA	ANDA076048	Apotex Corp	OMEPRAZOLE	10 mg/1	100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (60505-0145-2)
60505-0146-0	60505-0146	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20090121	20260331	ANDA	ANDA076048	Apotex Corp	OMEPRAZOLE	40 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (60505-0146-0)
60505-0146-1	60505-0146	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20090121	20270131	ANDA	ANDA076048	Apotex Corp	OMEPRAZOLE	40 mg/1	500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (60505-0146-1)
60505-0146-2	60505-0146	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20090121	20270131	ANDA	ANDA076048	Apotex Corp	OMEPRAZOLE	40 mg/1	100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (60505-0146-2)
60505-3952-8	60505-3952	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20031111	20270131	ANDA	ANDA076048	Apotex Corp	OMEPRAZOLE	20 mg/1	5000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (60505-3952-8)