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=ANDA075742"
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
55111-130-01 55111-130 HUMAN PRESCRIPTION DRUG Ranitidine Hydrochloride Ranitidine Hydrochloride CAPSULE ORAL 20010401 N/A ANDA ANDA075742 Dr. Reddy's Laboratories Limited RANITIDINE HYDROCHLORIDE 300 mg/1 100 CAPSULE in 1 BOTTLE (55111-130-01)
55111-130-30 55111-130 HUMAN PRESCRIPTION DRUG Ranitidine Hydrochloride Ranitidine Hydrochloride CAPSULE ORAL 20010401 N/A ANDA ANDA075742 Dr. Reddy's Laboratories Limited RANITIDINE HYDROCHLORIDE 300 mg/1 30 CAPSULE in 1 BOTTLE (55111-130-30)
55111-129-60 55111-129 HUMAN PRESCRIPTION DRUG Ranitidine Hydrochloride Ranitidine Hydrochloride CAPSULE ORAL 20010112 N/A ANDA ANDA075742 Dr. Reddy's Laboratories Limited RANITIDINE HYDROCHLORIDE 150 mg/1 60 CAPSULE in 1 BOTTLE (55111-129-60)
55111-129-05 55111-129 HUMAN PRESCRIPTION DRUG Ranitidine Hydrochloride Ranitidine Hydrochloride CAPSULE ORAL 20010112 N/A ANDA ANDA075742 Dr. Reddy's Laboratories Limited RANITIDINE HYDROCHLORIDE 150 mg/1 500 CAPSULE in 1 BOTTLE (55111-129-05)
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