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=ANDA206648"
符合检索条件的记录共 4 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
0703-0666-01 0703-0666 HUMAN PRESCRIPTION DRUG Treprostinil Treprostinil INJECTION, SOLUTION INTRAVENOUS; SUBCUTANEOUS 20190930 N/A ANDA ANDA206648 Teva Parenteral Medicines, Inc. TREPROSTINIL 20 mg/20mL 1 VIAL, MULTI-DOSE in 1 CARTON (0703-0666-01) / 20 mL in 1 VIAL, MULTI-DOSE
0703-0676-01 0703-0676 HUMAN PRESCRIPTION DRUG Treprostinil Treprostinil INJECTION, SOLUTION INTRAVENOUS; SUBCUTANEOUS 20190930 N/A ANDA ANDA206648 Teva Parenteral Medicines, Inc. TREPROSTINIL 50 mg/20mL 1 VIAL, MULTI-DOSE in 1 CARTON (0703-0676-01) / 20 mL in 1 VIAL, MULTI-DOSE
0703-0686-01 0703-0686 HUMAN PRESCRIPTION DRUG Treprostinil Treprostinil INJECTION, SOLUTION INTRAVENOUS; SUBCUTANEOUS 20190930 N/A ANDA ANDA206648 Teva Parenteral Medicines, Inc. TREPROSTINIL 100 mg/20mL 1 VIAL, MULTI-DOSE in 1 CARTON (0703-0686-01) / 20 mL in 1 VIAL, MULTI-DOSE
0703-0696-01 0703-0696 HUMAN PRESCRIPTION DRUG Treprostinil Treprostinil INJECTION, SOLUTION INTRAVENOUS; SUBCUTANEOUS 20190930 N/A ANDA ANDA206648 Teva Parenteral Medicines, Inc. TREPROSTINIL 200 mg/20mL 1 VIAL, MULTI-DOSE in 1 CARTON (0703-0696-01) / 20 mL in 1 VIAL, MULTI-DOSE
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