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=NDA021636"
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
68682-990-30 68682-990 HUMAN PRESCRIPTION DRUG Omeprazole and Sodium Bicarbonate omeprazole, sodium bicarbonate POWDER, FOR SUSPENSION ORAL 20040615 N/A NDA AUTHORIZED GENERIC NDA021636 Oceanside Pharmaceuticals OMEPRAZOLE; SODIUM BICARBONATE 20 mg/1; 1680 mg/1 30 PACKET in 1 CARTON (68682-990-30) / 1 POWDER, FOR SUSPENSION in 1 PACKET
68682-991-30 68682-991 HUMAN PRESCRIPTION DRUG Omeprazole and Sodium Bicarbonate omeprazole, sodium bicarbonate POWDER, FOR SUSPENSION ORAL 20040615 N/A NDA AUTHORIZED GENERIC NDA021636 Oceanside Pharmaceuticals OMEPRAZOLE; SODIUM BICARBONATE 40 mg/1; 1680 mg/1 30 PACKET in 1 CARTON (68682-991-30) / 1 POWDER, FOR SUSPENSION in 1 PACKET
68012-052-30 68012-052 HUMAN PRESCRIPTION DRUG ZEGERID omeprazole and sodium bicarbonate POWDER, FOR SUSPENSION ORAL 20040615 N/A NDA NDA021636 Santarus, Inc.. OMEPRAZOLE; SODIUM BICARBONATE 20 mg/1; 1680 mg/1 30 PACKET in 1 CARTON (68012-052-30) / 1 POWDER, FOR SUSPENSION in 1 PACKET
68012-054-03 68012-054 HUMAN PRESCRIPTION DRUG ZEGERID omeprazole and sodium bicarbonate POWDER, FOR SUSPENSION ORAL 20140615 N/A NDA NDA021636 Santarus, Inc.. OMEPRAZOLE; SODIUM BICARBONATE 40 mg/1; 1680 mg/1 3 PACKET in 1 CARTON (68012-054-03) / 1 POWDER, FOR SUSPENSION in 1 PACKET
68012-054-30 68012-054 HUMAN PRESCRIPTION DRUG ZEGERID omeprazole and sodium bicarbonate POWDER, FOR SUSPENSION ORAL 20140615 N/A NDA NDA021636 Santarus, Inc.. OMEPRAZOLE; SODIUM BICARBONATE 40 mg/1; 1680 mg/1 30 PACKET in 1 CARTON (68012-054-30) / 1 POWDER, FOR SUSPENSION in 1 PACKET
72162-1906-3 72162-1906 HUMAN PRESCRIPTION DRUG Omeprazole and Sodium Bicarbonate omeprazole, sodium bicarbonate POWDER, FOR SUSPENSION ORAL 20240321 N/A NDA AUTHORIZED GENERIC NDA021636 Bryant Ranch Prepack OMEPRAZOLE; SODIUM BICARBONATE 20 mg/1; 1680 mg/1 30 PACKET in 1 CARTON (72162-1906-3) / 1 POWDER, FOR SUSPENSION in 1 PACKET
72162-1907-3 72162-1907 HUMAN PRESCRIPTION DRUG Omeprazole and Sodium Bicarbonate omeprazole, sodium bicarbonate POWDER, FOR SUSPENSION ORAL 20240321 N/A NDA AUTHORIZED GENERIC NDA021636 Bryant Ranch Prepack OMEPRAZOLE; SODIUM BICARBONATE 40 mg/1; 1680 mg/1 30 PACKET in 1 CARTON (72162-1907-3) / 1 POWDER, FOR SUSPENSION in 1 PACKET
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