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=ANDA091416"
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
52959-193-30 52959-193 HUMAN PRESCRIPTION DRUG NAPROXEN NAPROXEN TABLET ORAL 20180102 N/A ANDA ANDA091416 H.J. Harkins Company., Inc. NAPROXEN 500 mg/1 30 TABLET in 1 CONTAINER (52959-193-30)
52959-193-40 52959-193 HUMAN PRESCRIPTION DRUG NAPROXEN NAPROXEN TABLET ORAL 20180102 N/A ANDA ANDA091416 H.J. Harkins Company., Inc. NAPROXEN 500 mg/1 40 TABLET in 1 CONTAINER (52959-193-40)
52959-193-45 52959-193 HUMAN PRESCRIPTION DRUG NAPROXEN NAPROXEN TABLET ORAL 20180102 N/A ANDA ANDA091416 H.J. Harkins Company., Inc. NAPROXEN 500 mg/1 45 TABLET in 1 CONTAINER (52959-193-45)
52959-193-60 52959-193 HUMAN PRESCRIPTION DRUG NAPROXEN NAPROXEN TABLET ORAL 20180102 N/A ANDA ANDA091416 H.J. Harkins Company., Inc. NAPROXEN 500 mg/1 60 TABLET in 1 CONTAINER (52959-193-60)
52959-193-90 52959-193 HUMAN PRESCRIPTION DRUG NAPROXEN NAPROXEN TABLET ORAL 20180102 N/A ANDA ANDA091416 H.J. Harkins Company., Inc. NAPROXEN 500 mg/1 90 TABLET in 1 CONTAINER (52959-193-90)
51655-621-20 51655-621 HUMAN PRESCRIPTION DRUG NAPROXEN NAPROXEN TABLET ORAL 20200706 N/A ANDA ANDA091416 Northwind Pharmaceuticals, LLC NAPROXEN 500 mg/1 20 TABLET in 1 BOTTLE, PLASTIC (51655-621-20)
51655-621-25 51655-621 HUMAN PRESCRIPTION DRUG NAPROXEN NAPROXEN TABLET ORAL 20200706 N/A ANDA ANDA091416 Northwind Pharmaceuticals, LLC NAPROXEN 500 mg/1 60 TABLET in 1 BOTTLE, PLASTIC (51655-621-25)
51655-621-83 51655-621 HUMAN PRESCRIPTION DRUG NAPROXEN NAPROXEN TABLET ORAL 20200706 N/A ANDA ANDA091416 Northwind Pharmaceuticals, LLC NAPROXEN 500 mg/1 180 TABLET in 1 BOTTLE, PLASTIC (51655-621-83)
76420-042-01 76420-042 HUMAN PRESCRIPTION DRUG NAPROXEN NAPROXEN TABLET ORAL 20200205 N/A ANDA ANDA091416 Asclemed USA, Inc. NAPROXEN 500 mg/1 1 TABLET in 1 BOTTLE, PLASTIC (76420-042-01)
76420-042-02 76420-042 HUMAN PRESCRIPTION DRUG NAPROXEN NAPROXEN TABLET ORAL 20200205 N/A ANDA ANDA091416 Asclemed USA, Inc. NAPROXEN 500 mg/1 2 TABLET in 1 BOTTLE, PLASTIC (76420-042-02)
76420-042-10 76420-042 HUMAN PRESCRIPTION DRUG NAPROXEN NAPROXEN TABLET ORAL 20200205 N/A ANDA ANDA091416 Asclemed USA, Inc. NAPROXEN 500 mg/1 100 TABLET in 1 BOTTLE, PLASTIC (76420-042-10)
76420-042-14 76420-042 HUMAN PRESCRIPTION DRUG NAPROXEN NAPROXEN TABLET ORAL 20200205 N/A ANDA ANDA091416 Asclemed USA, Inc. NAPROXEN 500 mg/1 14 TABLET in 1 BOTTLE, PLASTIC (76420-042-14)
52959-193-00 52959-193 HUMAN PRESCRIPTION DRUG NAPROXEN NAPROXEN TABLET ORAL 20180102 N/A ANDA ANDA091416 H.J. Harkins Company., Inc. NAPROXEN 500 mg/1 100 TABLET in 1 CONTAINER (52959-193-00)
52959-193-06 52959-193 HUMAN PRESCRIPTION DRUG NAPROXEN NAPROXEN TABLET ORAL 20180102 N/A ANDA ANDA091416 H.J. Harkins Company., Inc. NAPROXEN 500 mg/1 6 TABLET in 1 CONTAINER (52959-193-06)
52959-193-14 52959-193 HUMAN PRESCRIPTION DRUG NAPROXEN NAPROXEN TABLET ORAL 20180102 N/A ANDA ANDA091416 H.J. Harkins Company., Inc. NAPROXEN 500 mg/1 14 TABLET in 1 CONTAINER (52959-193-14)
76420-042-30 76420-042 HUMAN PRESCRIPTION DRUG NAPROXEN NAPROXEN TABLET ORAL 20200205 N/A ANDA ANDA091416 Asclemed USA, Inc. NAPROXEN 500 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (76420-042-30)
76420-042-60 76420-042 HUMAN PRESCRIPTION DRUG NAPROXEN NAPROXEN TABLET ORAL 20200205 N/A ANDA ANDA091416 Asclemed USA, Inc. NAPROXEN 500 mg/1 60 TABLET in 1 BOTTLE, PLASTIC (76420-042-60)
76420-042-90 76420-042 HUMAN PRESCRIPTION DRUG NAPROXEN NAPROXEN TABLET ORAL 20200205 N/A ANDA ANDA091416 Asclemed USA, Inc. NAPROXEN 500 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (76420-042-90)
25000-138-14 25000-138 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20110228 N/A ANDA ANDA091416 MARKSANS PHARMA LIMITED NAPROXEN 250 mg/1 1000 TABLET in 1 BOTTLE (25000-138-14)
25000-138-98 25000-138 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20110228 N/A ANDA ANDA091416 MARKSANS PHARMA LIMITED NAPROXEN 250 mg/1 1 BAG in 1 BOX (25000-138-98) / 37950 TABLET in 1 BAG
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