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=ANDA200166"
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
72162-1613-3 72162-1613 HUMAN PRESCRIPTION DRUG Amphetamine Sulfate Amphetamine Sulfate TABLET ORAL 20240701 N/A ANDA ANDA200166 Bryant Ranch Prepack AMPHETAMINE SULFATE 10 mg/1 30 TABLET in 1 BOTTLE (72162-1613-3)
72162-1612-3 72162-1612 HUMAN PRESCRIPTION DRUG Amphetamine Sulfate Amphetamine Sulfate TABLET ORAL 20240701 N/A ANDA ANDA200166 Bryant Ranch Prepack AMPHETAMINE SULFATE 5 mg/1 30 TABLET in 1 BOTTLE (72162-1612-3)
24338-026-03 24338-026 HUMAN PRESCRIPTION DRUG Evekeo Amphetamine Sulfate TABLET ORAL 20210312 N/A ANDA ANDA200166 AZURITY PHARMACEUTICALS, INC. AMPHETAMINE SULFATE 10 mg/1 30 TABLET in 1 BOTTLE (24338-026-03)
52536-059-03 52536-059 HUMAN PRESCRIPTION DRUG Amphetamine Sulfate Amphetamine Sulfate TABLET ORAL 20210107 N/A ANDA ANDA200166 Wilshire Pharmaceuticals AMPHETAMINE SULFATE 10 mg/1 30 TABLET in 1 BOTTLE (52536-059-03)
24338-022-03 24338-022 HUMAN PRESCRIPTION DRUG Evekeo Amphetamine Sulfate TABLET ORAL 20210312 N/A ANDA ANDA200166 AZURITY PHARMACEUTICALS, INC. AMPHETAMINE SULFATE 5 mg/1 30 TABLET in 1 BOTTLE (24338-022-03)
63629-2499-1 63629-2499 HUMAN PRESCRIPTION DRUG Amphetamine Sulfate Amphetamine Sulfate TABLET ORAL 20180329 N/A ANDA ANDA200166 Bryant Ranch Prepack AMPHETAMINE SULFATE 5 mg/1 100 TABLET in 1 BOTTLE (63629-2499-1)
52536-057-03 52536-057 HUMAN PRESCRIPTION DRUG Amphetamine Sulfate Amphetamine Sulfate TABLET ORAL 20210107 N/A ANDA ANDA200166 Wilshire Pharmaceuticals AMPHETAMINE SULFATE 5 mg/1 30 TABLET in 1 BOTTLE (52536-057-03)
63629-2498-1 63629-2498 HUMAN PRESCRIPTION DRUG Amphetamine Sulfate Amphetamine Sulfate TABLET ORAL 20180329 N/A ANDA ANDA200166 Bryant Ranch Prepack AMPHETAMINE SULFATE 10 mg/1 100 TABLET in 1 BOTTLE (63629-2498-1)
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