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）
检索条件:" 注册申请号=ANDA091352"
符合检索条件的记录共 49 条，共 3 页，当前第 2 页 ，可点击列名称排序
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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
65841-759-16 65841-759 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20121123 N/A ANDA ANDA091352 Zydus Lifesciences Limited OMEPRAZOLE 10 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65841-759-16)
65841-760-01 65841-760 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20121123 N/A ANDA ANDA091352 Zydus Lifesciences Limited OMEPRAZOLE 20 mg/1 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65841-760-01)
65841-760-05 65841-760 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20121123 N/A ANDA ANDA091352 Zydus Lifesciences Limited OMEPRAZOLE 20 mg/1 500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65841-760-05)
65841-760-06 65841-760 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20121123 N/A ANDA ANDA091352 Zydus Lifesciences Limited OMEPRAZOLE 20 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65841-760-06)
65841-760-10 65841-760 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20121123 N/A ANDA ANDA091352 Zydus Lifesciences Limited OMEPRAZOLE 20 mg/1 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65841-760-10)
65841-760-16 65841-760 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20121123 N/A ANDA ANDA091352 Zydus Lifesciences Limited OMEPRAZOLE 20 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65841-760-16)
65841-761-01 65841-761 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20121123 N/A ANDA ANDA091352 Zydus Lifesciences Limited OMEPRAZOLE 40 mg/1 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65841-761-01)
65841-761-05 65841-761 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20121123 N/A ANDA ANDA091352 Zydus Lifesciences Limited OMEPRAZOLE 40 mg/1 500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65841-761-05)
65841-761-06 65841-761 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20121123 N/A ANDA ANDA091352 Zydus Lifesciences Limited OMEPRAZOLE 40 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65841-761-06)
65841-761-10 65841-761 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20121123 N/A ANDA ANDA091352 Zydus Lifesciences Limited OMEPRAZOLE 40 mg/1 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65841-761-10)
65841-761-16 65841-761 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20121123 N/A ANDA ANDA091352 Zydus Lifesciences Limited OMEPRAZOLE 40 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65841-761-16)
50090-7018-0 50090-7018 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20240104 N/A ANDA ANDA091352 A-S Medication Solutions OMEPRAZOLE 20 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7018-0)
50090-7018-2 50090-7018 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20240104 N/A ANDA ANDA091352 A-S Medication Solutions OMEPRAZOLE 20 mg/1 15 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7018-2)
50090-7018-3 50090-7018 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20240104 N/A ANDA ANDA091352 A-S Medication Solutions OMEPRAZOLE 20 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7018-3)
50090-7018-4 50090-7018 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20240104 N/A ANDA ANDA091352 A-S Medication Solutions OMEPRAZOLE 20 mg/1 20 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7018-4)
50090-7018-5 50090-7018 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20240104 N/A ANDA ANDA091352 A-S Medication Solutions OMEPRAZOLE 20 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7018-5)
50090-7018-6 50090-7018 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20240104 N/A ANDA ANDA091352 A-S Medication Solutions OMEPRAZOLE 20 mg/1 200 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7018-6)
50090-7018-7 50090-7018 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20240104 N/A ANDA ANDA091352 A-S Medication Solutions OMEPRAZOLE 20 mg/1 180 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7018-7)
50090-7018-8 50090-7018 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20240104 N/A ANDA ANDA091352 A-S Medication Solutions OMEPRAZOLE 20 mg/1 7 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7018-8)
50090-7021-0 50090-7021 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20240104 N/A ANDA ANDA091352 A-S Medication Solutions OMEPRAZOLE 20 mg/1 100 BLISTER PACK in 1 CARTON (50090-7021-0) / 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK
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