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=ANDA213998"
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
70069-804-01 70069-804 HUMAN PRESCRIPTION DRUG Sumatriptan Sumatriptan INJECTION, SOLUTION SUBCUTANEOUS 20211025 N/A ANDA ANDA213998 Somerset Therapeutics, LLC SUMATRIPTAN SUCCINATE 6 mg/.5mL 1 VIAL in 1 CARTON (70069-804-01) / .5 mL in 1 VIAL
70069-804-05 70069-804 HUMAN PRESCRIPTION DRUG Sumatriptan Sumatriptan INJECTION, SOLUTION SUBCUTANEOUS 20211025 N/A ANDA ANDA213998 Somerset Therapeutics, LLC SUMATRIPTAN SUCCINATE 6 mg/.5mL 5 VIAL in 1 CARTON (70069-804-05) / .5 mL in 1 VIAL
65145-118-05 65145-118 HUMAN PRESCRIPTION DRUG Sumatriptan Sumatriptan INJECTION, SOLUTION SUBCUTANEOUS 20240928 N/A ANDA ANDA213998 Caplin Steriles Limited SUMATRIPTAN SUCCINATE 6 mg/.5mL 5 VIAL in 1 CARTON (65145-118-05) / .5 mL in 1 VIAL (65145-118-01)
70594-068-02 70594-068 HUMAN PRESCRIPTION DRUG Sumatriptan SUMATRIPTAN SUCCINATE INJECTION SUBCUTANEOUS 20220101 N/A ANDA ANDA213998 Xellia Pharmaceuticals USA LLC SUMATRIPTAN SUCCINATE 6 mg/.5mL 5 VIAL in 1 CARTON (70594-068-02) / .5 mL in 1 VIAL (70594-068-01)
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