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=ANDA217741"
符合检索条件的记录共 4 条，共 1 页，当前第 1 页 ，可点击列名称排序
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
70095-042-30 70095-042 HUMAN PRESCRIPTION DRUG Deflazacort Deflazacort TABLET ORAL 20250319 N/A ANDA ANDA217741 Sun Pharmaceutical Industries Limited DEFLAZACORT 30 mg/1 1 BOTTLE in 1 CARTON (70095-042-30) / 30 TABLET in 1 BOTTLE
70095-043-30 70095-043 HUMAN PRESCRIPTION DRUG Deflazacort Deflazacort TABLET ORAL 20250319 N/A ANDA ANDA217741 Sun Pharmaceutical Industries Limited DEFLAZACORT 36 mg/1 1 BOTTLE in 1 CARTON (70095-043-30) / 30 TABLET in 1 BOTTLE
70095-040-01 70095-040 HUMAN PRESCRIPTION DRUG Deflazacort Deflazacort TABLET ORAL 20250319 N/A ANDA ANDA217741 Sun Pharmaceutical Industries Limited DEFLAZACORT 6 mg/1 1 BOTTLE in 1 CARTON (70095-040-01) / 100 TABLET in 1 BOTTLE
70095-041-30 70095-041 HUMAN PRESCRIPTION DRUG Deflazacort Deflazacort TABLET ORAL 20250319 N/A ANDA ANDA217741 Sun Pharmaceutical Industries Limited DEFLAZACORT 18 mg/1 1 BOTTLE in 1 CARTON (70095-041-30) / 30 TABLET in 1 BOTTLE
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