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=ANDA212901"
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
63629-2078-1 63629-2078 HUMAN PRESCRIPTION DRUG AMPHETAMINE SULFATE amphetamine sulfate TABLET ORAL 20211221 N/A ANDA ANDA212901 Bryant Ranch Prepack AMPHETAMINE SULFATE 10 mg/1 100 TABLET in 1 BOTTLE (63629-2078-1)
63629-2079-1 63629-2079 HUMAN PRESCRIPTION DRUG AMPHETAMINE SULFATE amphetamine sulfate TABLET ORAL 20240402 N/A ANDA ANDA212901 Bryant Ranch Prepack AMPHETAMINE SULFATE 5 mg/1 100 TABLET in 1 BOTTLE (63629-2079-1)
72162-1087-1 72162-1087 HUMAN PRESCRIPTION DRUG AMPHETAMINE SULFATE amphetamine sulfate TABLET ORAL 20240405 N/A ANDA ANDA212901 Bryant Ranch Prepack AMPHETAMINE SULFATE 5 mg/1 100 TABLET in 1 BOTTLE (72162-1087-1)
72162-1088-1 72162-1088 HUMAN PRESCRIPTION DRUG AMPHETAMINE SULFATE amphetamine sulfate TABLET ORAL 20240405 N/A ANDA ANDA212901 Bryant Ranch Prepack AMPHETAMINE SULFATE 10 mg/1 100 TABLET in 1 BOTTLE (72162-1088-1)
0527-2524-37 0527-2524 HUMAN PRESCRIPTION DRUG AMPHETAMINE SULFATE amphetamine sulfate TABLET ORAL 20200601 N/A ANDA ANDA212901 Lannett Company, Inc. AMPHETAMINE SULFATE 5 mg/1 100 TABLET in 1 BOTTLE (0527-2524-37)
0527-2525-37 0527-2525 HUMAN PRESCRIPTION DRUG AMPHETAMINE SULFATE amphetamine sulfate TABLET ORAL 20200601 N/A ANDA ANDA212901 Lannett Company, Inc. AMPHETAMINE SULFATE 10 mg/1 100 TABLET in 1 BOTTLE (0527-2525-37)
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