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=ANDA203270"
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
57237-161-30 57237-161 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20150819 N/A ANDA ANDA203270 Rising Pharma Holdings, Inc. OMEPRAZOLE 20 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (57237-161-30)
57237-161-50 57237-161 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20150819 N/A ANDA ANDA203270 Rising Pharma Holdings, Inc. OMEPRAZOLE 20 mg/1 500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (57237-161-50)
57237-161-90 57237-161 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20150819 N/A ANDA ANDA203270 Rising Pharma Holdings, Inc. OMEPRAZOLE 20 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (57237-161-90)
57237-161-99 57237-161 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20150819 N/A ANDA ANDA203270 Rising Pharma Holdings, Inc. OMEPRAZOLE 20 mg/1 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (57237-161-99)
57237-162-01 57237-162 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20150819 N/A ANDA ANDA203270 Rising Pharma Holdings, Inc. OMEPRAZOLE 40 mg/1 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (57237-162-01)
57237-162-10 57237-162 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20150819 N/A ANDA ANDA203270 Rising Pharma Holdings, Inc. OMEPRAZOLE 40 mg/1 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (57237-162-10)
57237-162-30 57237-162 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20150819 N/A ANDA ANDA203270 Rising Pharma Holdings, Inc. OMEPRAZOLE 40 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (57237-162-30)
57237-162-50 57237-162 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20150819 N/A ANDA ANDA203270 Rising Pharma Holdings, Inc. OMEPRAZOLE 40 mg/1 500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (57237-162-50)
57237-162-90 57237-162 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20150819 N/A ANDA ANDA203270 Rising Pharma Holdings, Inc. OMEPRAZOLE 40 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (57237-162-90)
42708-159-14 42708-159 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20230301 N/A ANDA ANDA203270 QPharma, Inc. OMEPRAZOLE 40 mg/1 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (42708-159-14)
72162-2388-0 72162-2388 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20240828 N/A ANDA ANDA203270 Bryant Ranch Prepack OMEPRAZOLE 40 mg/1 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72162-2388-0)
72162-2388-2 72162-2388 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20240828 N/A ANDA ANDA203270 Bryant Ranch Prepack OMEPRAZOLE 40 mg/1 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72162-2388-2)
72162-2388-3 72162-2388 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20240828 N/A ANDA ANDA203270 Bryant Ranch Prepack OMEPRAZOLE 40 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72162-2388-3)
72162-2388-5 72162-2388 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20240828 N/A ANDA ANDA203270 Bryant Ranch Prepack OMEPRAZOLE 40 mg/1 500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72162-2388-5)
72162-2388-6 72162-2388 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20240828 N/A ANDA ANDA203270 Bryant Ranch Prepack OMEPRAZOLE 40 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72162-2388-6)
72162-2388-9 72162-2388 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20240828 N/A ANDA ANDA203270 Bryant Ranch Prepack OMEPRAZOLE 40 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72162-2388-9)
59651-001-01 59651-001 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20150819 N/A ANDA ANDA203270 Aurobindo Pharma Limited OMEPRAZOLE 10 mg/1 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (59651-001-01)
59651-001-03 59651-001 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20150819 N/A ANDA ANDA203270 Aurobindo Pharma Limited OMEPRAZOLE 10 mg/1 3 BLISTER PACK in 1 CARTON (59651-001-03) / 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (59651-001-10)
59651-001-30 59651-001 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20150819 N/A ANDA ANDA203270 Aurobindo Pharma Limited OMEPRAZOLE 10 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (59651-001-30)
59651-001-78 59651-001 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20150819 N/A ANDA ANDA203270 Aurobindo Pharma Limited OMEPRAZOLE 10 mg/1 10 BLISTER PACK in 1 CARTON (59651-001-78) / 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (59651-001-10)
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