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=ANDA207466"
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
71205-016-90 71205-016 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20180402 N/A ANDA ANDA207466 Proficient Rx LP METAXALONE 800 mg/1 90 TABLET in 1 BOTTLE (71205-016-90)
0276-0508-10 0276-0508 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20211101 N/A ANDA ANDA207466 Misemer Pharmaceuticals, Inc. METAXALONE 400 mg/1 100 TABLET in 1 BOTTLE (0276-0508-10)
50228-474-30 50228-474 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20200430 N/A ANDA ANDA207466 ScieGen Pharmaceuticals, Inc. METAXALONE 400 mg/1 30 TABLET in 1 BOTTLE (50228-474-30)
50228-474-10 50228-474 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20200430 N/A ANDA ANDA207466 ScieGen Pharmaceuticals, Inc. METAXALONE 400 mg/1 1000 TABLET in 1 BOTTLE (50228-474-10)
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