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
72789-482-14 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)
85509-1644-1 85509-1644 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20250729 N/A ANDA ANDA078490 PHOENIX RX LLC OMEPRAZOLE 20 mg/1 120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (85509-1644-1)
85509-1644-3 85509-1644 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20250729 N/A ANDA ANDA078490 PHOENIX RX LLC OMEPRAZOLE 20 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (85509-1644-3)
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)
68071-3733-2 68071-3733 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20250929 N/A ANDA ANDA078490 NuCare Pharmaceuticals, Inc. OMEPRAZOLE 20 mg/1 20 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68071-3733-2)
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)
60687-597-01 60687-597 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20251201 N/A ANDA ANDA078490 American Health Packaging OMEPRAZOLE 20 mg/1 100 BLISTER PACK in 1 CARTON (60687-597-01) / 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (60687-597-11)
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)
50090-7472-3 50090-7472 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20241212 N/A ANDA ANDA078490 A-S Medication Solutions OMEPRAZOLE 20 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7472-3)
50090-7472-4 50090-7472 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20241212 N/A ANDA ANDA078490 A-S Medication Solutions OMEPRAZOLE 20 mg/1 20 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7472-4)
16714-630-01 16714-630 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20260301 N/A ANDA ANDA078490 NorthStar Rx LLC OMEPRAZOLE 10 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (16714-630-01)
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)
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