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=ANDA091672"
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
70518-2251-1 70518-2251 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20241210 N/A ANDA ANDA091672 REMEDYREPACK INC. OMEPRAZOLE 20 mg/1 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-2251-1)
70518-2251-2 70518-2251 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20250129 N/A ANDA ANDA091672 REMEDYREPACK INC. OMEPRAZOLE 20 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-2251-2)
70518-2251-3 70518-2251 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20250318 N/A ANDA ANDA091672 REMEDYREPACK INC. OMEPRAZOLE 20 mg/1 100 POUCH in 1 BOX (70518-2251-3) / 1 CAPSULE, DELAYED RELEASE in 1 POUCH (70518-2251-4)
70518-2251-5 70518-2251 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20250817 N/A ANDA ANDA091672 REMEDYREPACK INC. OMEPRAZOLE 20 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (70518-2251-5)
85509-1396-1 85509-1396 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20250723 N/A ANDA ANDA091672 PHOENIX RX LLC OMEPRAZOLE 20 mg/1 120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (85509-1396-1)
85509-1396-2 85509-1396 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20250723 N/A ANDA ANDA091672 PHOENIX RX LLC OMEPRAZOLE 20 mg/1 20 CAPSULE, DELAYED RELEASE in 1 BOTTLE (85509-1396-2)
85509-1396-3 85509-1396 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20250723 N/A ANDA ANDA091672 PHOENIX RX LLC OMEPRAZOLE 20 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (85509-1396-3)
85509-1396-6 85509-1396 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20250723 N/A ANDA ANDA091672 PHOENIX RX LLC OMEPRAZOLE 20 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (85509-1396-6)
85509-1396-9 85509-1396 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20250723 N/A ANDA ANDA091672 PHOENIX RX LLC OMEPRAZOLE 20 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (85509-1396-9)
68788-6881-1 68788-6881 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20170120 N/A ANDA ANDA091672 Preferred Pharmaceuticals Inc. OMEPRAZOLE 20 mg/1 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-6881-1)
68788-6881-2 68788-6881 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20170120 N/A ANDA ANDA091672 Preferred Pharmaceuticals Inc. OMEPRAZOLE 20 mg/1 20 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-6881-2)
68788-6881-3 68788-6881 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20170120 N/A ANDA ANDA091672 Preferred Pharmaceuticals Inc. OMEPRAZOLE 20 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-6881-3)
68788-6881-4 68788-6881 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20170120 N/A ANDA ANDA091672 Preferred Pharmaceuticals Inc. OMEPRAZOLE 20 mg/1 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-6881-4)
68788-6881-6 68788-6881 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20170120 N/A ANDA ANDA091672 Preferred Pharmaceuticals Inc. OMEPRAZOLE 20 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-6881-6)
68788-6881-8 68788-6881 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20170120 N/A ANDA ANDA091672 Preferred Pharmaceuticals Inc. OMEPRAZOLE 20 mg/1 120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-6881-8)
68788-6881-9 68788-6881 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20170120 N/A ANDA ANDA091672 Preferred Pharmaceuticals Inc. OMEPRAZOLE 20 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-6881-9)
68788-6995-1 68788-6995 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20171027 N/A ANDA ANDA091672 Preferred Pharmaceuticals Inc. OMEPRAZOLE 40 mg/1 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-6995-1)
68788-6995-3 68788-6995 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20171027 N/A ANDA ANDA091672 Preferred Pharmaceuticals Inc. OMEPRAZOLE 40 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-6995-3)
68788-6995-6 68788-6995 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20171027 N/A ANDA ANDA091672 Preferred Pharmaceuticals Inc. OMEPRAZOLE 40 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-6995-6)
68788-6995-8 68788-6995 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20171027 N/A ANDA ANDA091672 Preferred Pharmaceuticals Inc. OMEPRAZOLE 40 mg/1 120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-6995-8)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2025 Drugfuture->U.S. FDA National Drug Code DataBase