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 50 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)
65841-759-06 65841-759 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20121123 N/A ANDA ANDA091352 Zydus Lifesciences Limited OMEPRAZOLE 10 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65841-759-06)
65841-759-05 65841-759 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20121123 N/A ANDA ANDA091352 Zydus Lifesciences Limited OMEPRAZOLE 10 mg/1 500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65841-759-05)
65841-759-01 65841-759 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20121123 N/A ANDA ANDA091352 Zydus Lifesciences Limited OMEPRAZOLE 10 mg/1 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65841-759-01)
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)
65841-761-16 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)
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)
68382-411-01 68382-411 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20121123 N/A ANDA ANDA091352 Zydus Pharmaceuticals USA Inc. OMEPRAZOLE 10 mg/1 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68382-411-01)
68382-411-05 68382-411 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20121123 N/A ANDA ANDA091352 Zydus Pharmaceuticals USA Inc. OMEPRAZOLE 10 mg/1 500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68382-411-05)
68382-411-06 68382-411 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20121123 N/A ANDA ANDA091352 Zydus Pharmaceuticals USA Inc. OMEPRAZOLE 10 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68382-411-06)
68382-411-10 68382-411 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20121123 N/A ANDA ANDA091352 Zydus Pharmaceuticals USA Inc. OMEPRAZOLE 10 mg/1 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68382-411-10)
68382-411-16 68382-411 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20121123 N/A ANDA ANDA091352 Zydus Pharmaceuticals USA Inc. OMEPRAZOLE 10 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68382-411-16)
68382-412-01 68382-412 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20121123 N/A ANDA ANDA091352 Zydus Pharmaceuticals USA Inc. OMEPRAZOLE 20 mg/1 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68382-412-01)
68382-412-05 68382-412 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20121123 N/A ANDA ANDA091352 Zydus Pharmaceuticals USA Inc. OMEPRAZOLE 20 mg/1 500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68382-412-05)
68382-412-06 68382-412 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20121123 N/A ANDA ANDA091352 Zydus Pharmaceuticals USA Inc. OMEPRAZOLE 20 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68382-412-06)
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