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=ANDA213510"
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
25021-254-08 25021-254 HUMAN PRESCRIPTION DRUG Docetaxel Docetaxel Anhydrous INJECTION INTRAVENOUS 20230801 N/A ANDA ANDA213510 Sagent Pharmaceuticals DOCETAXEL ANHYDROUS 10 mg/mL 1 VIAL in 1 CARTON (25021-254-08) / 8 mL in 1 VIAL
25021-254-16 25021-254 HUMAN PRESCRIPTION DRUG Docetaxel Docetaxel Anhydrous INJECTION INTRAVENOUS 20230801 N/A ANDA ANDA213510 Sagent Pharmaceuticals DOCETAXEL ANHYDROUS 10 mg/mL 1 VIAL in 1 CARTON (25021-254-16) / 16 mL in 1 VIAL
68083-400-01 68083-400 HUMAN PRESCRIPTION DRUG Docetaxel Docetaxel INJECTION INTRAVENOUS 20210701 N/A ANDA ANDA213510 Gland Pharma Limited DOCETAXEL ANHYDROUS 10 mg/mL 1 VIAL, MULTI-DOSE in 1 CARTON (68083-400-01) / 8 mL in 1 VIAL, MULTI-DOSE
68083-401-01 68083-401 HUMAN PRESCRIPTION DRUG Docetaxel Docetaxel INJECTION INTRAVENOUS 20210701 N/A ANDA ANDA213510 Gland Pharma Limited DOCETAXEL ANHYDROUS 10 mg/mL 1 VIAL, MULTI-DOSE in 1 CARTON (68083-401-01) / 16 mL in 1 VIAL, MULTI-DOSE
68083-399-01 68083-399 HUMAN PRESCRIPTION DRUG Docetaxel Docetaxel INJECTION INTRAVENOUS 20210701 N/A ANDA ANDA213510 Gland Pharma Limited DOCETAXEL ANHYDROUS 10 mg/mL 1 VIAL, SINGLE-DOSE in 1 CARTON (68083-399-01) / 2 mL in 1 VIAL, SINGLE-DOSE
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