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=ANDA210050"
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
0093-7769-24 0093-7769 HUMAN PRESCRIPTION DRUG Everolimus Everolimus TABLET ORAL 20231023 N/A ANDA ANDA210050 Teva Pharmaceuticals USA, Inc. EVEROLIMUS 10 mg/1 28 BLISTER PACK in 1 CARTON (0093-7769-24) / 1 TABLET in 1 BLISTER PACK (0093-7769-19)
0093-7768-24 0093-7768 HUMAN PRESCRIPTION DRUG Everolimus Everolimus TABLET ORAL 20200610 N/A ANDA ANDA210050 Teva Pharmaceuticals USA, Inc. EVEROLIMUS 7.5 mg/1 28 BLISTER PACK in 1 CARTON (0093-7768-24) / 1 TABLET in 1 BLISTER PACK (0093-7768-19)
0093-7767-24 0093-7767 HUMAN PRESCRIPTION DRUG Everolimus Everolimus TABLET ORAL 20200610 N/A ANDA ANDA210050 Teva Pharmaceuticals USA, Inc. EVEROLIMUS 5 mg/1 28 BLISTER PACK in 1 CARTON (0093-7767-24) / 1 TABLET in 1 BLISTER PACK (0093-7767-19)
0093-7766-24 0093-7766 HUMAN PRESCRIPTION DRUG Everolimus Everolimus TABLET ORAL 20200610 N/A ANDA ANDA210050 Teva Pharmaceuticals USA, Inc. EVEROLIMUS 2.5 mg/1 28 BLISTER PACK in 1 CARTON (0093-7766-24) / 1 TABLET in 1 BLISTER PACK (0093-7766-19)
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