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=ANDA216729"
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
72266-261-01 72266-261 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium LEVOTHYROXINE SODIUM ANHYDROUS INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION INTRAVENOUS 20250918 N/A ANDA ANDA216729 Fosun Pharma USA Inc. LEVOTHYROXINE SODIUM ANHYDROUS 100 ug/5mL 1 VIAL, SINGLE-DOSE in 1 CARTON (72266-261-01) / 5 mL in 1 VIAL, SINGLE-DOSE
83270-008-01 83270-008 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium LEVOTHYROXINE SODIUM ANHYDROUS INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION INTRAVENOUS 20250930 N/A ANDA ANDA216729 ONESOURCE SPECIALTY PHARMA LIMITED LEVOTHYROXINE SODIUM ANHYDROUS 500 ug/5mL 1 VIAL, SINGLE-DOSE in 1 CARTON (83270-008-01) / 5 mL in 1 VIAL, SINGLE-DOSE
83270-006-01 83270-006 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium LEVOTHYROXINE SODIUM ANHYDROUS INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION INTRAVENOUS 20250930 N/A ANDA ANDA216729 ONESOURCE SPECIALTY PHARMA LIMITED LEVOTHYROXINE SODIUM ANHYDROUS 100 ug/5mL 1 VIAL, SINGLE-DOSE in 1 CARTON (83270-006-01) / 5 mL in 1 VIAL, SINGLE-DOSE
83270-007-01 83270-007 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium LEVOTHYROXINE SODIUM ANHYDROUS INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION INTRAVENOUS 20250930 N/A ANDA ANDA216729 ONESOURCE SPECIALTY PHARMA LIMITED LEVOTHYROXINE SODIUM ANHYDROUS 200 ug/5mL 1 VIAL, SINGLE-DOSE in 1 CARTON (83270-007-01) / 5 mL in 1 VIAL, SINGLE-DOSE
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