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=ANDA078881"
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
43353-265-09 43353-265 HUMAN PRESCRIPTION DRUG Ropinirole Hydrochloride ropinirole TABLET ORAL 20161201 N/A ANDA ANDA078881 Aphena Pharma Solutions - Tennessee, LLC ROPINIROLE HYDROCHLORIDE .5 mg/1 9000 TABLET in 1 BOTTLE, PLASTIC (43353-265-09)
43353-266-09 43353-266 HUMAN PRESCRIPTION DRUG Ropinirole Hydrochloride ropinirole TABLET ORAL 20161202 N/A ANDA ANDA078881 Aphena Pharma Solutions - Tennessee, LLC ROPINIROLE HYDROCHLORIDE 1 mg/1 9000 TABLET in 1 BOTTLE, PLASTIC (43353-266-09)
43353-267-09 43353-267 HUMAN PRESCRIPTION DRUG Ropinirole Hydrochloride ropinirole TABLET ORAL 20161202 N/A ANDA ANDA078881 Aphena Pharma Solutions - Tennessee, LLC ROPINIROLE HYDROCHLORIDE 2 mg/1 9000 TABLET in 1 BOTTLE, PLASTIC (43353-267-09)
43353-258-09 43353-258 HUMAN PRESCRIPTION DRUG Ropinirole Hydrochloride ropinirole TABLET ORAL 20161115 N/A ANDA ANDA078881 Aphena Pharma Solutions - Tennessee, LLC ROPINIROLE HYDROCHLORIDE .25 mg/1 9000 TABLET in 1 BOTTLE, PLASTIC (43353-258-09)
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