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=ANDA209035"
符合检索条件的记录共 5 条，共 1 页，当前第 1 页 ，可点击列名称排序
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
67046-1452-3 67046-1452 HUMAN PRESCRIPTION DRUG Amantadine Hydrochloride Amantadine Hydrochloride TABLET ORAL 20250207 N/A ANDA ANDA209035 Coupler LLC AMANTADINE HYDROCHLORIDE 100 mg/1 30 TABLET in 1 BLISTER PACK (67046-1452-3)
42543-497-05 42543-497 HUMAN PRESCRIPTION DRUG Amantadine Hydrochloride Amantadine Hydrochloride TABLET ORAL 20170808 N/A ANDA ANDA209035 Strides Pharma Inc. AMANTADINE HYDROCHLORIDE 100 mg/1 500 TABLET in 1 BOTTLE (42543-497-05)
42543-497-01 42543-497 HUMAN PRESCRIPTION DRUG Amantadine Hydrochloride Amantadine Hydrochloride TABLET ORAL 20170804 N/A ANDA ANDA209035 Strides Pharma Inc. AMANTADINE HYDROCHLORIDE 100 mg/1 100 TABLET in 1 BOTTLE (42543-497-01)
72189-535-30 72189-535 HUMAN PRESCRIPTION DRUG Amantadine HCL Amantadine HCL TABLET ORAL 20240223 N/A ANDA ANDA209035 Direct_Rx AMANTADINE HYDROCHLORIDE 100 mg/1 30 TABLET in 1 BOTTLE (72189-535-30)
72189-535-90 72189-535 HUMAN PRESCRIPTION DRUG Amantadine HCL Amantadine HCL TABLET ORAL 20240223 N/A ANDA ANDA209035 Direct_Rx AMANTADINE HYDROCHLORIDE 100 mg/1 90 TABLET in 1 BOTTLE (72189-535-90)
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