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
68788-8771-8 68788-8771 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20241120 N/A ANDA ANDA078490 Preferred Pharmaceuticals Inc. OMEPRAZOLE 40 mg/1 120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8771-8)
68788-8771-9 68788-8771 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20241120 N/A ANDA ANDA078490 Preferred Pharmaceuticals Inc. OMEPRAZOLE 40 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8771-9)
68788-8805-1 68788-8805 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20250120 N/A ANDA ANDA078490 Preferred Pharmaceuticals Inc. OMEPRAZOLE 20 mg/1 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8805-1)
68788-8805-2 68788-8805 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20250120 N/A ANDA ANDA078490 Preferred Pharmaceuticals Inc. OMEPRAZOLE 20 mg/1 20 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8805-2)
68788-8805-3 68788-8805 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20250120 N/A ANDA ANDA078490 Preferred Pharmaceuticals Inc. OMEPRAZOLE 20 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8805-3)
68788-8805-4 68788-8805 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20250120 N/A ANDA ANDA078490 Preferred Pharmaceuticals Inc. OMEPRAZOLE 20 mg/1 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8805-4)
68788-8805-6 68788-8805 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20250120 N/A ANDA ANDA078490 Preferred Pharmaceuticals Inc. OMEPRAZOLE 20 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8805-6)
68788-8805-7 68788-8805 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20250120 N/A ANDA ANDA078490 Preferred Pharmaceuticals Inc. OMEPRAZOLE 20 mg/1 120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8805-7)
68788-8805-9 68788-8805 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20250120 N/A ANDA ANDA078490 Preferred Pharmaceuticals Inc. OMEPRAZOLE 20 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8805-9)
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)
50268-657-15 50268-657 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20230322 N/A ANDA ANDA078490 AvPAK OMEPRAZOLE 40 mg/1 50 BLISTER PACK in 1 BOX (50268-657-15) / 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (50268-657-11)
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