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=ANDA074140"
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
70518-3726-0 70518-3726 HUMAN PRESCRIPTION DRUG Naproxen Naproxen Sodium TABLET ORAL 20230430 N/A ANDA ANDA074140 REMEDYREPACK INC. NAPROXEN SODIUM 500 mg/1 30 TABLET in 1 BLISTER PACK (70518-3726-0)
70518-3726-1 70518-3726 HUMAN PRESCRIPTION DRUG Naproxen Naproxen Sodium TABLET ORAL 20230524 N/A ANDA ANDA074140 REMEDYREPACK INC. NAPROXEN SODIUM 500 mg/1 6 TABLET in 1 BLISTER PACK (70518-3726-1)
70518-3726-2 70518-3726 HUMAN PRESCRIPTION DRUG Naproxen Naproxen Sodium TABLET ORAL 20230524 N/A ANDA ANDA074140 REMEDYREPACK INC. NAPROXEN SODIUM 500 mg/1 14 TABLET in 1 BOTTLE, PLASTIC (70518-3726-2)
70518-3726-3 70518-3726 HUMAN PRESCRIPTION DRUG Naproxen Naproxen Sodium TABLET ORAL 20230608 N/A ANDA ANDA074140 REMEDYREPACK INC. NAPROXEN SODIUM 500 mg/1 60 TABLET in 1 BOTTLE, PLASTIC (70518-3726-3)
70518-3726-4 70518-3726 HUMAN PRESCRIPTION DRUG Naproxen Naproxen Sodium TABLET ORAL 20230612 N/A ANDA ANDA074140 REMEDYREPACK INC. NAPROXEN SODIUM 500 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (70518-3726-4)
70518-3726-5 70518-3726 HUMAN PRESCRIPTION DRUG Naproxen Naproxen Sodium TABLET ORAL 20230621 N/A ANDA ANDA074140 REMEDYREPACK INC. NAPROXEN SODIUM 500 mg/1 20 TABLET in 1 BOTTLE, PLASTIC (70518-3726-5)
70518-3748-0 70518-3748 HUMAN PRESCRIPTION DRUG Naproxen Naproxen Sodium TABLET ORAL 20230606 N/A ANDA ANDA074140 REMEDYREPACK INC. NAPROXEN SODIUM 250 mg/1 30 TABLET in 1 BLISTER PACK (70518-3748-0)
70518-3748-1 70518-3748 HUMAN PRESCRIPTION DRUG Naproxen Naproxen Sodium TABLET ORAL 20240403 N/A ANDA ANDA074140 REMEDYREPACK INC. NAPROXEN SODIUM 250 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (70518-3748-1)
70010-137-01 70010-137 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20210415 N/A ANDA ANDA074140 Granules Pharmaceuticals Inc. NAPROXEN 250 mg/1 100 TABLET in 1 BOTTLE (70010-137-01)
70010-137-05 70010-137 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20210415 N/A ANDA ANDA074140 Granules Pharmaceuticals Inc. NAPROXEN 250 mg/1 500 TABLET in 1 BOTTLE (70010-137-05)
70010-137-10 70010-137 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20210415 N/A ANDA ANDA074140 Granules Pharmaceuticals Inc. NAPROXEN 250 mg/1 1000 TABLET in 1 BOTTLE (70010-137-10)
70010-138-01 70010-138 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20210415 N/A ANDA ANDA074140 Granules Pharmaceuticals Inc. NAPROXEN 375 mg/1 100 TABLET in 1 BOTTLE (70010-138-01)
70010-138-05 70010-138 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20210415 N/A ANDA ANDA074140 Granules Pharmaceuticals Inc. NAPROXEN 375 mg/1 500 TABLET in 1 BOTTLE (70010-138-05)
70010-138-10 70010-138 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20210415 N/A ANDA ANDA074140 Granules Pharmaceuticals Inc. NAPROXEN 375 mg/1 1000 TABLET in 1 BOTTLE (70010-138-10)
70010-139-01 70010-139 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20210415 N/A ANDA ANDA074140 Granules Pharmaceuticals Inc. NAPROXEN 500 mg/1 100 TABLET in 1 BOTTLE (70010-139-01)
70010-139-05 70010-139 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20210415 N/A ANDA ANDA074140 Granules Pharmaceuticals Inc. NAPROXEN 500 mg/1 500 TABLET in 1 BOTTLE (70010-139-05)
70010-139-10 70010-139 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20210415 N/A ANDA ANDA074140 Granules Pharmaceuticals Inc. NAPROXEN 500 mg/1 1000 TABLET in 1 BOTTLE (70010-139-10)
51655-457-20 51655-457 HUMAN PRESCRIPTION DRUG Naproxen Naproxen Sodium TABLET ORAL 20230703 N/A ANDA ANDA074140 Northwind Pharmaceuticals, LLC NAPROXEN SODIUM 500 mg/1 20 TABLET in 1 BOTTLE, PLASTIC (51655-457-20)
51655-457-25 51655-457 HUMAN PRESCRIPTION DRUG Naproxen Naproxen Sodium TABLET ORAL 20230504 N/A ANDA ANDA074140 Northwind Pharmaceuticals, LLC NAPROXEN SODIUM 500 mg/1 60 TABLET in 1 BOTTLE, PLASTIC (51655-457-25)
51655-457-26 51655-457 HUMAN PRESCRIPTION DRUG Naproxen Naproxen Sodium TABLET ORAL 20230615 N/A ANDA ANDA074140 Northwind Pharmaceuticals, LLC NAPROXEN SODIUM 500 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (51655-457-26)
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