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=ANDA209713"
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
50090-5792-1 50090-5792 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20211011 N/A ANDA ANDA209713 A-S Medication Solutions LEVOTHYROXINE SODIUM .137 mg/1 30 TABLET in 1 BOTTLE (50090-5792-1)
68071-3956-9 68071-3956 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20260123 N/A ANDA ANDA209713 NuCare Pharmaceuticals, Inc. LEVOTHYROXINE SODIUM .025 mg/1 90 TABLET in 1 BOTTLE (68071-3956-9)
50090-6569-0 50090-6569 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20230731 N/A ANDA ANDA209713 A-S Medication Solutions LEVOTHYROXINE SODIUM .05 mg/1 30 TABLET in 1 BOTTLE (50090-6569-0)
50090-6569-1 50090-6569 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20230731 N/A ANDA ANDA209713 A-S Medication Solutions LEVOTHYROXINE SODIUM .05 mg/1 90 TABLET in 1 BOTTLE (50090-6569-1)
50090-6572-0 50090-6572 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20230801 N/A ANDA ANDA209713 A-S Medication Solutions LEVOTHYROXINE SODIUM .05 mg/1 90 TABLET in 1 BOTTLE (50090-6572-0)
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