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=NDA019071"
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
44523-415-01 44523-415 HUMAN PRESCRIPTION DRUG Potassium Citrate potassium citrate TABLET ORAL 20131223 N/A NDA AUTHORIZED GENERIC NDA019071 Biocomp Pharma, Inc. POTASSIUM CITRATE 15 meq/1 100 TABLET in 1 BOTTLE (44523-415-01)
0245-0071-11 0245-0071 HUMAN PRESCRIPTION DRUG Potassium Citrate potassium citrate TABLET ORAL 20060901 N/A NDA NDA019071 Upsher-Smith Laboratories, LLC POTASSIUM CITRATE 10 meq/1 100 TABLET in 1 BOTTLE (0245-0071-11)
0245-0070-11 0245-0070 HUMAN PRESCRIPTION DRUG Potassium Citrate potassium citrate TABLET ORAL 20060901 N/A NDA NDA019071 Upsher-Smith Laboratories, LLC POTASSIUM CITRATE 5 meq/1 100 TABLET in 1 BOTTLE (0245-0070-11)
0178-0610-01 0178-0610 HUMAN PRESCRIPTION DRUG UROCIT-K potassium citrate TABLET, EXTENDED RELEASE ORAL 20091230 N/A NDA NDA019071 Mission Pharmacal Company POTASSIUM CITRATE 10 meq/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0178-0610-01)
0178-0600-01 0178-0600 HUMAN PRESCRIPTION DRUG UROCIT-K potassium citrate TABLET, EXTENDED RELEASE ORAL 20091230 N/A NDA NDA019071 Mission Pharmacal Company POTASSIUM CITRATE 5 meq/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0178-0600-01)
0178-0615-01 0178-0615 HUMAN PRESCRIPTION DRUG UROCIT-K potassium citrate TABLET, EXTENDED RELEASE ORAL 20100127 N/A NDA NDA019071 Mission Pharmacal Company POTASSIUM CITRATE 15 meq/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0178-0615-01)
72162-2187-1 72162-2187 HUMAN PRESCRIPTION DRUG Potassium Citrate potassium citrate TABLET ORAL 20240403 N/A NDA AUTHORIZED GENERIC NDA019071 Bryant Ranch Prepack POTASSIUM CITRATE 15 meq/1 100 TABLET in 1 BOTTLE (72162-2187-1)
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