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
68382-503-04	68382-503	HUMAN OTC DRUG	omeprazole and sodium bicarbonate	omeprazole and sodium bicarbonate	CAPSULE	ORAL	20180719	N/A	ANDA	ANDA203345	Zydus Pharmaceuticals USA Inc.	OMEPRAZOLE; SODIUM BICARBONATE	20 mg/1; 1100 mg/1	3 BOTTLE in 1 CARTON (68382-503-04) / 14 CAPSULE in 1 BOTTLE
68382-503-17	68382-503	HUMAN OTC DRUG	omeprazole and sodium bicarbonate	omeprazole and sodium bicarbonate	CAPSULE	ORAL	20180719	N/A	ANDA	ANDA203345	Zydus Pharmaceuticals USA Inc.	OMEPRAZOLE; SODIUM BICARBONATE	20 mg/1; 1100 mg/1	2 BOTTLE in 1 CARTON (68382-503-17) / 14 CAPSULE in 1 BOTTLE
68382-503-67	68382-503	HUMAN OTC DRUG	omeprazole and sodium bicarbonate	omeprazole and sodium bicarbonate	CAPSULE	ORAL	20180719	N/A	ANDA	ANDA203345	Zydus Pharmaceuticals USA Inc.	OMEPRAZOLE; SODIUM BICARBONATE	20 mg/1; 1100 mg/1	1 BOTTLE in 1 CARTON (68382-503-67) / 14 CAPSULE in 1 BOTTLE
70771-1337-4	70771-1337	HUMAN OTC DRUG	omeprazole and sodium bicarbonate	omeprazole and sodium bicarbonate	CAPSULE	ORAL	20180719	N/A	ANDA	ANDA203345	Zydus Lifesciences Limited	OMEPRAZOLE; SODIUM BICARBONATE	20 mg/1; 1100 mg/1	3 BOTTLE in 1 CARTON (70771-1337-4) / 14 CAPSULE in 1 BOTTLE
70771-1337-7	70771-1337	HUMAN OTC DRUG	omeprazole and sodium bicarbonate	omeprazole and sodium bicarbonate	CAPSULE	ORAL	20180719	N/A	ANDA	ANDA203345	Zydus Lifesciences Limited	OMEPRAZOLE; SODIUM BICARBONATE	20 mg/1; 1100 mg/1	1 BOTTLE in 1 CARTON (70771-1337-7) / 14 CAPSULE in 1 BOTTLE
70771-1337-8	70771-1337	HUMAN OTC DRUG	omeprazole and sodium bicarbonate	omeprazole and sodium bicarbonate	CAPSULE	ORAL	20180719	N/A	ANDA	ANDA203345	Zydus Lifesciences Limited	OMEPRAZOLE; SODIUM BICARBONATE	20 mg/1; 1100 mg/1	2 BOTTLE in 1 CARTON (70771-1337-8) / 14 CAPSULE in 1 BOTTLE