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=ANDA091280"
符合检索条件的记录共 3 条，共 1 页，当前第 1 页 ，可点击列名称排序
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
16714-015-01 16714-015 HUMAN PRESCRIPTION DRUG Desmopressin Acetate Desmopressin Acetate INJECTION, SOLUTION INTRAVENOUS; SUBCUTANEOUS 20200701 N/A ANDA ANDA091280 NorthStar RxLLC DESMOPRESSIN ACETATE 4 ug/mL 1 VIAL in 1 CARTON (16714-015-01) / 10 mL in 1 VIAL
62756-529-40 62756-529 HUMAN PRESCRIPTION DRUG Desmopressin Acetate Desmopressin Acetate INJECTION, SOLUTION INTRAVENOUS; SUBCUTANEOUS 20130130 N/A ANDA ANDA091280 Sun Pharmaceutical Industries, Inc. DESMOPRESSIN ACETATE 4 ug/mL 1 VIAL in 1 CARTON (62756-529-40) / 10 mL in 1 VIAL
62756-529-26 62756-529 HUMAN PRESCRIPTION DRUG desmopressin acetate desmopressin acetate INJECTION, SOLUTION INTRAVENOUS; SUBCUTANEOUS 20140220 N/A ANDA ANDA091280 Sun Pharmaceutical Industries, Inc. DESMOPRESSIN ACETATE 4 ug/mL 1 VIAL, MULTI-DOSE in 1 CARTON (62756-529-26) / 10 mL in 1 VIAL, MULTI-DOSE
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