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=ANDA088276"
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
68071-2730-9 68071-2730 HUMAN PRESCRIPTION DRUG Imipramine Hydrochloride Imipramine Hydrochloride TABLET ORAL 20220523 N/A ANDA ANDA088276 NuCare Pharmaceuticals,Inc. IMIPRAMINE HYDROCHLORIDE 50 mg/1 90 TABLET in 1 BOTTLE (68071-2730-9)
60429-097-01 60429-097 HUMAN PRESCRIPTION DRUG Imipramine Hydrochloride Imipramine Hydrochloride TABLET ORAL 19990827 20240831 ANDA ANDA088276 Golden State Medical Supply, Inc. IMIPRAMINE HYDROCHLORIDE 50 mg/1 100 TABLET in 1 BOTTLE (60429-097-01)
64380-171-02 64380-171 HUMAN PRESCRIPTION DRUG Imipramine Hydrochloride Imipramine Hydrochloride TABLET ORAL 20220411 N/A ANDA ANDA088276 Strides Pharma Science Limited IMIPRAMINE HYDROCHLORIDE 50 mg/1 1000 TABLET in 1 BOTTLE, PLASTIC (64380-171-02)
64380-171-01 64380-171 HUMAN PRESCRIPTION DRUG Imipramine Hydrochloride Imipramine Hydrochloride TABLET ORAL 20220411 N/A ANDA ANDA088276 Strides Pharma Science Limited IMIPRAMINE HYDROCHLORIDE 50 mg/1 100 TABLET in 1 BOTTLE, PLASTIC (64380-171-01)
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