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=ANDA216922"
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
68083-550-10 68083-550 HUMAN PRESCRIPTION DRUG Desmopressin Acetate Desmopressin Acetate INJECTION, SOLUTION INTRAVENOUS; SUBCUTANEOUS 20221116 N/A ANDA ANDA216922 Gland Pharma Limited DESMOPRESSIN ACETATE 4 ug/mL 10 VIAL, SINGLE-DOSE in 1 CARTON (68083-550-10) / 1 mL in 1 VIAL, SINGLE-DOSE (68083-550-01)
65219-293-01 65219-293 HUMAN PRESCRIPTION DRUG Desmopressin Acetate Desmopressin Acetate INJECTION, SOLUTION INTRAVENOUS; SUBCUTANEOUS 20230911 N/A ANDA ANDA216922 Fresenius Kabi USA, LLC DESMOPRESSIN ACETATE 4 ug/mL 10 VIAL, SINGLE-DOSE in 1 CARTON (65219-293-01) / 1 mL in 1 VIAL, SINGLE-DOSE (65219-293-00)
70095-026-02 70095-026 HUMAN PRESCRIPTION DRUG Desmopressin Acetate Desmopressin Acetate INJECTION, SOLUTION INTRAVENOUS; SUBCUTANEOUS 20230403 N/A ANDA ANDA216922 Sun Pharmaceutical Industries Limited DESMOPRESSIN ACETATE 4 ug/mL 10 VIAL, SINGLE-DOSE in 1 CARTON (70095-026-02) / 1 mL in 1 VIAL, SINGLE-DOSE (70095-026-01)
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