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=ANDA202038"
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
65862-560-99 65862-560 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20120928 N/A ANDA ANDA202038 Aurobindo Pharma Limited PANTOPRAZOLE SODIUM 40 mg/1 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-560-99)
70518-1788-0 70518-1788 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20190111 N/A ANDA ANDA202038 REMEDYREPACK INC. PANTOPRAZOLE SODIUM 20 mg/1 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-1788-0)
70518-1788-1 70518-1788 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20190501 N/A ANDA ANDA202038 REMEDYREPACK INC. PANTOPRAZOLE SODIUM 20 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-1788-1)
70934-102-30 70934-102 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20190529 20250630 ANDA ANDA202038 Denton Pharma, Inc. DBA Northwind Pharmaceuticals PANTOPRAZOLE SODIUM 40 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70934-102-30)
70934-861-30 70934-861 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20210525 20240930 ANDA ANDA202038 Denton Pharma, Inc. DBA Northwind Pharmaceuticals PANTOPRAZOLE SODIUM 20 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70934-861-30)
0904-6870-45 0904-6870 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20120928 N/A ANDA ANDA202038 Major Pharmaceuticals PANTOPRAZOLE SODIUM 40 mg/1 80 BLISTER PACK in 1 CARTON (0904-6870-45) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK
51655-075-25 51655-075 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20240223 N/A ANDA ANDA202038 Northwind Pharmaceuticals, LLC PANTOPRAZOLE SODIUM 20 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (51655-075-25)
51655-075-52 51655-075 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20220927 N/A ANDA ANDA202038 Northwind Pharmaceuticals, LLC PANTOPRAZOLE SODIUM 20 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (51655-075-52)
35573-428-80 35573-428 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20200420 N/A ANDA ANDA202038 Burel Pharmaceuticals, LLC PANTOPRAZOLE SODIUM 40 mg/1 10 BLISTER PACK in 1 CARTON (35573-428-80) / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK
50090-5361-0 50090-5361 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20201113 N/A ANDA ANDA202038 A-S Medication Solutions PANTOPRAZOLE SODIUM 20 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-5361-0)
50090-5361-1 50090-5361 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20201113 N/A ANDA ANDA202038 A-S Medication Solutions PANTOPRAZOLE SODIUM 20 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-5361-1)
50090-5361-2 50090-5361 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20201113 N/A ANDA ANDA202038 A-S Medication Solutions PANTOPRAZOLE SODIUM 20 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-5361-2)
42708-185-30 42708-185 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20240112 N/A ANDA ANDA202038 QPharma Inc PANTOPRAZOLE SODIUM 40 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (42708-185-30)
50090-5378-0 50090-5378 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20201119 N/A ANDA ANDA202038 A-S Medication Solutions PANTOPRAZOLE SODIUM 40 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-5378-0)
50090-5378-1 50090-5378 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20201119 N/A ANDA ANDA202038 A-S Medication Solutions PANTOPRAZOLE SODIUM 40 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-5378-1)
50090-5379-0 50090-5379 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20201119 N/A ANDA ANDA202038 A-S Medication Solutions PANTOPRAZOLE SODIUM 40 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-5379-0)
51655-797-52 51655-797 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20220221 N/A ANDA ANDA202038 Northwind Pharmaceuticals, LLC PANTOPRAZOLE SODIUM 40 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (51655-797-52)
71335-0310-1 71335-0310 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20190307 N/A ANDA ANDA202038 Bryant Ranch Prepack PANTOPRAZOLE SODIUM 40 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0310-1)
71335-0310-2 71335-0310 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20190313 N/A ANDA ANDA202038 Bryant Ranch Prepack PANTOPRAZOLE SODIUM 40 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0310-2)
71335-0310-3 71335-0310 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20190401 N/A ANDA ANDA202038 Bryant Ranch Prepack PANTOPRAZOLE SODIUM 40 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0310-3)
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