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=ANDA076511"
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
67296-2056-3 67296-2056 HUMAN PRESCRIPTION DRUG Finasteride Finasteride TABLET, FILM COATED ORAL 20061215 N/A ANDA ANDA076511 RedPharm Drug FINASTERIDE 5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (67296-2056-3)
0093-7355-05 0093-7355 HUMAN PRESCRIPTION DRUG Finasteride Finasteride TABLET, FILM COATED ORAL 20080314 N/A ANDA ANDA076511 Teva Pharmaceuticals USA, Inc. FINASTERIDE 5 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (0093-7355-05)
0093-7355-56 0093-7355 HUMAN PRESCRIPTION DRUG Finasteride Finasteride TABLET, FILM COATED ORAL 20061215 N/A ANDA ANDA076511 Teva Pharmaceuticals USA, Inc. FINASTERIDE 5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (0093-7355-56)
0093-7355-98 0093-7355 HUMAN PRESCRIPTION DRUG Finasteride Finasteride TABLET, FILM COATED ORAL 20070222 N/A ANDA ANDA076511 Teva Pharmaceuticals USA, Inc. FINASTERIDE 5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (0093-7355-98)
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