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=ANDA219477"
符合检索条件的记录共 6 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
43598-887-30 43598-887 HUMAN PRESCRIPTION DRUG Prednisone delayed release Prednisone TABLET, DELAYED RELEASE ORAL 20251215 N/A ANDA ANDA219477 Dr. Reddys Laboratories Inc. PREDNISONE 2 mg/1 1 BOTTLE in 1 CARTON (43598-887-30) / 30 TABLET, DELAYED RELEASE in 1 BOTTLE
74157-010-30 74157-010 HUMAN PRESCRIPTION DRUG Prednisone delayed release Prednisone TABLET, DELAYED RELEASE ORAL 20251215 N/A ANDA ANDA219477 INA Pharmaceutics Inc PREDNISONE 1 mg/1 1 BOTTLE in 1 CARTON (74157-010-30) / 30 TABLET, DELAYED RELEASE in 1 BOTTLE
74157-019-30 74157-019 HUMAN PRESCRIPTION DRUG Prednisone delayed release Prednisone TABLET, DELAYED RELEASE ORAL 20251215 N/A ANDA ANDA219477 INA Pharmaceutics Inc PREDNISONE 2 mg/1 1 BOTTLE in 1 CARTON (74157-019-30) / 30 TABLET, DELAYED RELEASE in 1 BOTTLE
43598-887-01 43598-887 HUMAN PRESCRIPTION DRUG Prednisone delayed release Prednisone TABLET, DELAYED RELEASE ORAL 20251215 N/A ANDA ANDA219477 Dr. Reddys Laboratories Inc. PREDNISONE 2 mg/1 1 BOTTLE in 1 CARTON (43598-887-01) / 100 TABLET, DELAYED RELEASE in 1 BOTTLE
43598-886-30 43598-886 HUMAN PRESCRIPTION DRUG Prednisone delayed release Prednisone TABLET, DELAYED RELEASE ORAL 20251215 N/A ANDA ANDA219477 Dr. Reddys Laboratories Inc. PREDNISONE 1 mg/1 1 BOTTLE in 1 CARTON (43598-886-30) / 30 TABLET, DELAYED RELEASE in 1 BOTTLE
43598-886-01 43598-886 HUMAN PRESCRIPTION DRUG Prednisone delayed release Prednisone TABLET, DELAYED RELEASE ORAL 20251215 N/A ANDA ANDA219477 Dr. Reddys Laboratories Inc. PREDNISONE 1 mg/1 1 BOTTLE in 1 CARTON (43598-886-01) / 100 TABLET, DELAYED RELEASE in 1 BOTTLE
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