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=ANDA216904"
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
68083-549-01 68083-549 HUMAN PRESCRIPTION DRUG Desmopressin Acetate Desmopressin Acetate INJECTION, SOLUTION INTRAVENOUS; SUBCUTANEOUS 20230320 N/A ANDA ANDA216904 Gland Pharma Limited DESMOPRESSIN ACETATE 4 ug/mL 1 VIAL, MULTI-DOSE in 1 CARTON (68083-549-01) / 10 mL in 1 VIAL, MULTI-DOSE
65219-295-10 65219-295 HUMAN PRESCRIPTION DRUG Desmopressin Acetate Desmopressin Acetate INJECTION, SOLUTION INTRAVENOUS; SUBCUTANEOUS 20230911 N/A ANDA ANDA216904 Fresenius Kabi USA, LLC DESMOPRESSIN ACETATE 4 ug/mL 1 VIAL, MULTI-DOSE in 1 CARTON (65219-295-10) / 10 mL in 1 VIAL, MULTI-DOSE
70095-031-01 70095-031 HUMAN PRESCRIPTION DRUG Desmopressin Acetate Desmopressin Acetate INJECTION, SOLUTION INTRAVENOUS; SUBCUTANEOUS 20230620 N/A ANDA ANDA216904 Sun Pharmaceutical Industries Limited DESMOPRESSIN ACETATE 4 ug/mL 1 VIAL in 1 CARTON (70095-031-01) / 10 mL in 1 VIAL
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