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
71335-0217-4 71335-0217 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20240905 N/A ANDA ANDA078250 Bryant Ranch Prepack NAPROXEN 250 mg/1 120 TABLET in 1 BOTTLE (71335-0217-4)
71335-0217-5 71335-0217 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20240905 N/A ANDA ANDA078250 Bryant Ranch Prepack NAPROXEN 250 mg/1 10 TABLET in 1 BOTTLE (71335-0217-5)
71335-0217-6 71335-0217 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20240905 N/A ANDA ANDA078250 Bryant Ranch Prepack NAPROXEN 250 mg/1 90 TABLET in 1 BOTTLE (71335-0217-6)
71335-0217-7 71335-0217 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20240905 N/A ANDA ANDA078250 Bryant Ranch Prepack NAPROXEN 250 mg/1 40 TABLET in 1 BOTTLE (71335-0217-7)
71335-0217-8 71335-0217 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20240905 N/A ANDA ANDA078250 Bryant Ranch Prepack NAPROXEN 250 mg/1 45 TABLET in 1 BOTTLE (71335-0217-8)
67296-0406-1 67296-0406 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20070701 N/A ANDA ANDA078250 RedPharm Drug, Inc. NAPROXEN 500 mg/1 30 TABLET in 1 BOTTLE (67296-0406-1)
67296-0406-2 67296-0406 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20070701 N/A ANDA ANDA078250 RedPharm Drug, Inc. NAPROXEN 500 mg/1 60 TABLET in 1 BOTTLE (67296-0406-2)
67296-0406-3 67296-0406 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20070701 N/A ANDA ANDA078250 RedPharm Drug, Inc. NAPROXEN 500 mg/1 20 TABLET in 1 BOTTLE (67296-0406-3)
67296-0406-4 67296-0406 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20070701 N/A ANDA ANDA078250 RedPharm Drug, Inc. NAPROXEN 500 mg/1 6 TABLET in 1 BOTTLE (67296-0406-4)
67296-0406-7 67296-0406 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20070701 N/A ANDA ANDA078250 RedPharm Drug, Inc. NAPROXEN 500 mg/1 14 TABLET in 1 BOTTLE (67296-0406-7)
61919-162-30 61919-162 HUMAN PRESCRIPTION DRUG NAPROXEN NAPROXEN TABLET ORAL 20160829 N/A ANDA ANDA078250 DIRECT RX NAPROXEN 375 mg/1 30 TABLET in 1 BOTTLE (61919-162-30)
61919-162-60 61919-162 HUMAN PRESCRIPTION DRUG NAPROXEN NAPROXEN TABLET ORAL 20160829 N/A ANDA ANDA078250 DIRECT RX NAPROXEN 375 mg/1 60 TABLET in 1 BOTTLE (61919-162-60)
68462-188-01 68462-188 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20070701 N/A ANDA ANDA078250 Glenmark Pharmaceuticals Inc., USA NAPROXEN 250 mg/1 100 TABLET in 1 BOTTLE (68462-188-01)
68462-188-05 68462-188 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20070701 N/A ANDA ANDA078250 Glenmark Pharmaceuticals Inc., USA NAPROXEN 250 mg/1 500 TABLET in 1 BOTTLE (68462-188-05)
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)
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)
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