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=ANDA076436"
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
55111-171-30 55111-171 HUMAN PRESCRIPTION DRUG Finasteride Finasteride TABLET, FILM COATED ORAL 20130102 N/A ANDA ANDA076436 Dr. Reddy's Laboratories Limited FINASTERIDE 1 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (55111-171-30)
55111-171-90 55111-171 HUMAN PRESCRIPTION DRUG Finasteride Finasteride TABLET, FILM COATED ORAL 20130102 N/A ANDA ANDA076436 Dr. Reddy's Laboratories Limited FINASTERIDE 1 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (55111-171-90)
55111-171-18 55111-171 HUMAN PRESCRIPTION DRUG Finasteride Finasteride TABLET, FILM COATED ORAL 20130102 N/A ANDA ANDA076436 Dr. Reddy's Laboratories Limited FINASTERIDE 1 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (55111-171-18)
55111-171-05 55111-171 HUMAN PRESCRIPTION DRUG Finasteride Finasteride TABLET, FILM COATED ORAL 20130102 N/A ANDA ANDA076436 Dr. Reddy's Laboratories Limited FINASTERIDE 1 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (55111-171-05)
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