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=ANDA078250"
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
71335-0095-4 71335-0095 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20260519 N/A ANDA ANDA078250 Bryant Ranch Prepack NAPROXEN 375 mg/1 120 TABLET in 1 BOTTLE (71335-0095-4)
71335-0095-5 71335-0095 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20260519 N/A ANDA ANDA078250 Bryant Ranch Prepack NAPROXEN 375 mg/1 60 TABLET in 1 BOTTLE (71335-0095-5)
71335-0095-6 71335-0095 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20260519 N/A ANDA ANDA078250 Bryant Ranch Prepack NAPROXEN 375 mg/1 90 TABLET in 1 BOTTLE (71335-0095-6)
71335-0095-7 71335-0095 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20260519 N/A ANDA ANDA078250 Bryant Ranch Prepack NAPROXEN 375 mg/1 14 TABLET in 1 BOTTLE (71335-0095-7)
71335-0095-8 71335-0095 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20260519 N/A ANDA ANDA078250 Bryant Ranch Prepack NAPROXEN 375 mg/1 15 TABLET in 1 BOTTLE (71335-0095-8)
68462-190-01 68462-190 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20070701 N/A ANDA ANDA078250 Glenmark Pharmaceuticals Inc., USA NAPROXEN 500 mg/1 100 TABLET in 1 BOTTLE (68462-190-01)
68462-190-05 68462-190 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20070701 N/A ANDA ANDA078250 Glenmark Pharmaceuticals Inc., USA NAPROXEN 500 mg/1 500 TABLET in 1 BOTTLE (68462-190-05)
68462-190-30 68462-190 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20070701 N/A ANDA ANDA078250 Glenmark Pharmaceuticals Inc., USA NAPROXEN 500 mg/1 30 TABLET in 1 BOTTLE (68462-190-30)
68462-190-50 68462-190 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20070701 N/A ANDA ANDA078250 Glenmark Pharmaceuticals Inc., USA NAPROXEN 500 mg/1 50 TABLET in 1 BOTTLE (68462-190-50)
71335-0095-9 71335-0095 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20260519 N/A ANDA ANDA078250 Bryant Ranch Prepack NAPROXEN 375 mg/1 21 TABLET in 1 BOTTLE (71335-0095-9)
66267-153-30 66267-153 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20161010 N/A ANDA ANDA078250 NuCare Pharmaceuticals, Inc. NAPROXEN 500 mg/1 30 TABLET in 1 BOTTLE (66267-153-30)
68462-189-01 68462-189 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20070701 N/A ANDA ANDA078250 Glenmark Pharmaceuticals Inc., USA NAPROXEN 375 mg/1 100 TABLET in 1 BOTTLE (68462-189-01)
68462-189-05 68462-189 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20070701 N/A ANDA ANDA078250 Glenmark Pharmaceuticals Inc., USA NAPROXEN 375 mg/1 500 TABLET in 1 BOTTLE (68462-189-05)
66267-153-40 66267-153 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20161010 N/A ANDA ANDA078250 NuCare Pharmaceuticals, Inc. NAPROXEN 500 mg/1 40 TABLET in 1 BOTTLE (66267-153-40)
66267-153-42 66267-153 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20161010 N/A ANDA ANDA078250 NuCare Pharmaceuticals, Inc. NAPROXEN 500 mg/1 42 TABLET in 1 BOTTLE (66267-153-42)
66267-153-60 66267-153 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20161010 N/A ANDA ANDA078250 NuCare Pharmaceuticals, Inc. NAPROXEN 500 mg/1 60 TABLET in 1 BOTTLE (66267-153-60)
66267-153-90 66267-153 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20161010 N/A ANDA ANDA078250 NuCare Pharmaceuticals, Inc. NAPROXEN 500 mg/1 90 TABLET in 1 BOTTLE (66267-153-90)
68788-8797-1 68788-8797 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20250101 N/A ANDA ANDA078250 Preferred Pharmaceuticals Inc. NAPROXEN 500 mg/1 100 TABLET in 1 BOTTLE (68788-8797-1)
68788-8797-2 68788-8797 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20250101 N/A ANDA ANDA078250 Preferred Pharmaceuticals Inc. NAPROXEN 500 mg/1 20 TABLET in 1 BOTTLE (68788-8797-2)
68788-8797-3 68788-8797 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20250101 N/A ANDA ANDA078250 Preferred Pharmaceuticals Inc. NAPROXEN 500 mg/1 30 TABLET in 1 BOTTLE (68788-8797-3)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase