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=ANDA217021"
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
70436-116-82 70436-116 HUMAN PRESCRIPTION DRUG Leucovorin Calcium leucovorin calcium INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION INTRAMUSCULAR; INTRAVENOUS 20230710 N/A ANDA ANDA217021 Slate Run Pharmaceuticals, LLC LEUCOVORIN CALCIUM 50 mg/1 10 VIAL in 1 BOX (70436-116-82) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (70436-116-80)
70436-117-80 70436-117 HUMAN PRESCRIPTION DRUG Leucovorin Calcium leucovorin calcium INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION INTRAMUSCULAR; INTRAVENOUS 20230710 N/A ANDA ANDA217021 Slate Run Pharmaceuticals, LLC LEUCOVORIN CALCIUM 100 mg/1 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (70436-117-80)
70436-118-80 70436-118 HUMAN PRESCRIPTION DRUG Leucovorin Calcium leucovorin calcium INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION INTRAMUSCULAR; INTRAVENOUS 20230710 N/A ANDA ANDA217021 Slate Run Pharmaceuticals, LLC LEUCOVORIN CALCIUM 200 mg/1 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (70436-118-80)
70436-120-80 70436-120 HUMAN PRESCRIPTION DRUG Leucovorin Calcium leucovorin calcium INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION INTRAMUSCULAR; INTRAVENOUS 20230710 N/A ANDA ANDA217021 Slate Run Pharmaceuticals, LLC LEUCOVORIN CALCIUM 500 mg/1 500 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (70436-120-80)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase