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
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)
72789-482-90 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)
67046-1509-3 67046-1509 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20250129 N/A ANDA ANDA078490 Coupler LLC OMEPRAZOLE 20 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (67046-1509-3)
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)
50090-6721-0 50090-6721 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20231005 N/A ANDA ANDA078490 A-S Medication Solutions OMEPRAZOLE 40 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-6721-0)
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)
80425-0109-1 80425-0109 HUMAN PRESCRIPTION DRUG Omeprazole DR Omeprazole CAPSULE, DELAYED RELEASE ORAL 20191025 N/A ANDA ANDA078490 Advanced Rx Pharmacy of Tennessee, LLC OMEPRAZOLE 40 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0109-1)
82009-023-05 82009-023 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20221115 N/A ANDA ANDA078490 Quallent Pharmaceuticals Health LLC OMEPRAZOLE 40 mg/1 500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (82009-023-05)
83008-077-90 83008-077 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20240813 20260131 ANDA ANDA078490 Quality Care Products, LLC OMEPRAZOLE 20 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (83008-077-90)
83008-077-60 83008-077 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20240813 20260131 ANDA ANDA078490 Quality Care Products, LLC OMEPRAZOLE 20 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (83008-077-60)
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