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=ANDA217696"
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
70954-402-10 70954-402 HUMAN PRESCRIPTION DRUG Dexamethasone Dexamethasone TABLET ORAL 20230509 N/A ANDA ANDA217696 ANI Pharmaceuticals, Inc. DEXAMETHASONE 2 mg/1 100 TABLET in 1 BOTTLE (70954-402-10)
72603-188-01 72603-188 HUMAN PRESCRIPTION DRUG Dexamethasone Dexamethasone TABLET ORAL 20230807 N/A ANDA ANDA217696 NorthStar Rx LLC DEXAMETHASONE 2 mg/1 100 TABLET in 1 BOTTLE (72603-188-01)
72189-523-08 72189-523 HUMAN PRESCRIPTION DRUG Dexamethasone Dexamethasone TABLET ORAL 20231113 N/A ANDA ANDA217696 Direct_Rx DEXAMETHASONE 2 mg/1 8 TABLET in 1 BOTTLE (72189-523-08)
60687-773-01 60687-773 HUMAN PRESCRIPTION DRUG Dexamethasone Dexamethasone TABLET ORAL 20231101 N/A ANDA ANDA217696 American Health Packaging DEXAMETHASONE 2 mg/1 100 BLISTER PACK in 1 CARTON (60687-773-01) / 1 TABLET in 1 BLISTER PACK (60687-773-11)
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