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=ANDA078490"
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
85509-1644-6 85509-1644 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20250729 N/A ANDA ANDA078490 PHOENIX RX LLC OMEPRAZOLE 20 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (85509-1644-6)
85509-1644-9 85509-1644 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20250729 N/A ANDA ANDA078490 PHOENIX RX LLC OMEPRAZOLE 20 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (85509-1644-9)
80425-0504-1 80425-0504 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20250306 N/A ANDA ANDA078490 Advanced Rx of Tennessee, LLC OMEPRAZOLE 20 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0504-1)
80425-0504-2 80425-0504 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20250306 N/A ANDA ANDA078490 Advanced Rx of Tennessee, LLC OMEPRAZOLE 20 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0504-2)
80425-0504-3 80425-0504 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20250306 N/A ANDA ANDA078490 Advanced Rx of Tennessee, LLC OMEPRAZOLE 20 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0504-3)
80425-0504-4 80425-0504 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20250306 N/A ANDA ANDA078490 Advanced Rx of Tennessee, LLC OMEPRAZOLE 20 mg/1 120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0504-4)
68071-2741-3 68071-2741 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20220602 N/A ANDA ANDA078490 NuCare Pharmaceuticals,Inc. OMEPRAZOLE 40 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68071-2741-3)
72789-482-14 72789-482 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20250507 N/A ANDA ANDA078490 PD-Rx Pharmaceuticals, Inc. OMEPRAZOLE 20 mg/1 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72789-482-14)
72789-482-30 72789-482 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20250125 N/A ANDA ANDA078490 PD-Rx Pharmaceuticals, Inc. OMEPRAZOLE 20 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72789-482-30)
72789-482-60 72789-482 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20250320 N/A ANDA ANDA078490 PD-Rx Pharmaceuticals, Inc. OMEPRAZOLE 20 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72789-482-60)
72789-482-90 72789-482 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20250123 N/A ANDA ANDA078490 PD-Rx Pharmaceuticals, Inc. OMEPRAZOLE 20 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72789-482-90)
50090-6720-0 50090-6720 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20231005 N/A ANDA ANDA078490 A-S Medication Solutions OMEPRAZOLE 40 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-6720-0)
50090-6720-1 50090-6720 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20231115 N/A ANDA ANDA078490 A-S Medication Solutions OMEPRAZOLE 40 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-6720-1)
50090-6720-2 50090-6720 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20231115 N/A ANDA ANDA078490 A-S Medication Solutions OMEPRAZOLE 40 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-6720-2)
50090-7472-0 50090-7472 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20241212 N/A ANDA ANDA078490 A-S Medication Solutions OMEPRAZOLE 20 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7472-0)
50090-7472-2 50090-7472 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20241212 N/A ANDA ANDA078490 A-S Medication Solutions OMEPRAZOLE 20 mg/1 15 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7472-2)
50090-7474-0 50090-7474 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20241212 N/A ANDA ANDA078490 A-S Medication Solutions OMEPRAZOLE 20 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7474-0)
60687-608-01 60687-608 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20210804 N/A ANDA ANDA078490 American Health Packaging OMEPRAZOLE 40 mg/1 100 BLISTER PACK in 1 CARTON (60687-608-01) / 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (60687-608-11)
16714-123-01 16714-123 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20191025 N/A ANDA ANDA078490 NorthStar Rx LLC OMEPRAZOLE 40 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (16714-123-01)
16714-123-02 16714-123 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20191025 N/A ANDA ANDA078490 NorthStar Rx LLC OMEPRAZOLE 40 mg/1 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (16714-123-02)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase