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
70771-1102-4	70771-1102	HUMAN PRESCRIPTION DRUG	omeprazole and sodium bicarbonate	omeprazole and sodium bicarbonate	CAPSULE	ORAL	20180529	N/A	ANDA	ANDA203290	Zydus Lifesciences Limited	OMEPRAZOLE; SODIUM BICARBONATE	40 mg/1; 1100 mg/1	10 BLISTER PACK in 1 CARTON (70771-1102-4) / 10 CAPSULE in 1 BLISTER PACK (70771-1102-2)
70771-1102-5	70771-1102	HUMAN PRESCRIPTION DRUG	omeprazole and sodium bicarbonate	omeprazole and sodium bicarbonate	CAPSULE	ORAL	20180529	N/A	ANDA	ANDA203290	Zydus Lifesciences Limited	OMEPRAZOLE; SODIUM BICARBONATE	40 mg/1; 1100 mg/1	500 CAPSULE in 1 BOTTLE (70771-1102-5)
70771-1102-9	70771-1102	HUMAN PRESCRIPTION DRUG	omeprazole and sodium bicarbonate	omeprazole and sodium bicarbonate	CAPSULE	ORAL	20180529	N/A	ANDA	ANDA203290	Zydus Lifesciences Limited	OMEPRAZOLE; SODIUM BICARBONATE	40 mg/1; 1100 mg/1	90 CAPSULE in 1 BOTTLE (70771-1102-9)
70771-1101-3	70771-1101	HUMAN PRESCRIPTION DRUG	omeprazole and sodium bicarbonate	omeprazole and sodium bicarbonate	CAPSULE	ORAL	20180529	N/A	ANDA	ANDA203290	Zydus Lifesciences Limited	OMEPRAZOLE; SODIUM BICARBONATE	20 mg/1; 1100 mg/1	30 CAPSULE in 1 BOTTLE (70771-1101-3)
70771-1101-4	70771-1101	HUMAN PRESCRIPTION DRUG	omeprazole and sodium bicarbonate	omeprazole and sodium bicarbonate	CAPSULE	ORAL	20180529	N/A	ANDA	ANDA203290	Zydus Lifesciences Limited	OMEPRAZOLE; SODIUM BICARBONATE	20 mg/1; 1100 mg/1	10 BLISTER PACK in 1 CARTON (70771-1101-4) / 10 CAPSULE in 1 BLISTER PACK (70771-1101-2)
70771-1101-0	70771-1101	HUMAN PRESCRIPTION DRUG	omeprazole and sodium bicarbonate	omeprazole and sodium bicarbonate	CAPSULE	ORAL	20180529	N/A	ANDA	ANDA203290	Zydus Lifesciences Limited	OMEPRAZOLE; SODIUM BICARBONATE	20 mg/1; 1100 mg/1	1000 CAPSULE in 1 BOTTLE (70771-1101-0)