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
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)
70010-138-05 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)
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)
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)
51655-457-52 51655-457 HUMAN PRESCRIPTION DRUG Naproxen Naproxen Sodium TABLET ORAL 20230504 N/A ANDA ANDA074140 Northwind Pharmaceuticals, LLC NAPROXEN SODIUM 500 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (51655-457-52)
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)
70010-138-01 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)
82868-030-30 82868-030 HUMAN PRESCRIPTION DRUG Naproxen Naproxen Sodium TABLET ORAL 20231212 N/A ANDA ANDA074140 Northwind Pharmaceuticals, LLC NAPROXEN SODIUM 375 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (82868-030-30)
62207-745-49 62207-745 HUMAN PRESCRIPTION DRUG Naproxen Naproxen Sodium TABLET ORAL 20210415 N/A ANDA ANDA074140 Granules India Ltd NAPROXEN SODIUM 250 mg/1 1000 TABLET in 1 BOTTLE (62207-745-49)
62207-745-43 62207-745 HUMAN PRESCRIPTION DRUG Naproxen Naproxen Sodium TABLET ORAL 20210415 N/A ANDA ANDA074140 Granules India Ltd NAPROXEN SODIUM 250 mg/1 100 TABLET in 1 BOTTLE (62207-745-43)
62207-746-43 62207-746 HUMAN PRESCRIPTION DRUG Naproxen Naproxen Sodium TABLET ORAL 20210415 N/A ANDA ANDA074140 Granules India Ltd NAPROXEN SODIUM 375 mg/1 100 TABLET in 1 BOTTLE (62207-746-43)
62207-745-47 62207-745 HUMAN PRESCRIPTION DRUG Naproxen Naproxen Sodium TABLET ORAL 20210415 N/A ANDA ANDA074140 Granules India Ltd NAPROXEN SODIUM 250 mg/1 500 TABLET in 1 BOTTLE (62207-745-47)
62207-746-49 62207-746 HUMAN PRESCRIPTION DRUG Naproxen Naproxen Sodium TABLET ORAL 20210415 N/A ANDA ANDA074140 Granules India Ltd NAPROXEN SODIUM 375 mg/1 1000 TABLET in 1 BOTTLE (62207-746-49)
62207-747-49 62207-747 HUMAN PRESCRIPTION DRUG Naproxen Naproxen Sodium TABLET ORAL 20210415 N/A ANDA ANDA074140 Granules India Ltd NAPROXEN SODIUM 500 mg/1 1000 TABLET in 1 BOTTLE (62207-747-49)
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