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=ANDA209151"
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
13668-453-01 13668-453 HUMAN PRESCRIPTION DRUG anagrelide anagrelide CAPSULE ORAL 20170630 N/A ANDA ANDA209151 Torrent Pharmaceuticals Limited ANAGRELIDE HYDROCHLORIDE ANHYDROUS .5 mg/1 100 CAPSULE in 1 BOTTLE (13668-453-01)
13668-453-30 13668-453 HUMAN PRESCRIPTION DRUG anagrelide anagrelide CAPSULE ORAL 20170630 N/A ANDA ANDA209151 Torrent Pharmaceuticals Limited ANAGRELIDE HYDROCHLORIDE ANHYDROUS .5 mg/1 30 CAPSULE in 1 BOTTLE (13668-453-30)
13668-462-01 13668-462 HUMAN PRESCRIPTION DRUG anagrelide anagrelide CAPSULE ORAL 20170630 N/A ANDA ANDA209151 Torrent Pharmaceuticals Limited ANAGRELIDE HYDROCHLORIDE ANHYDROUS 1 mg/1 100 CAPSULE in 1 BOTTLE (13668-462-01)
13668-462-30 13668-462 HUMAN PRESCRIPTION DRUG anagrelide anagrelide CAPSULE ORAL 20170630 N/A ANDA ANDA209151 Torrent Pharmaceuticals Limited ANAGRELIDE HYDROCHLORIDE ANHYDROUS 1 mg/1 30 CAPSULE in 1 BOTTLE (13668-462-30)
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