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=NDA014134"
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
83703-036-01 83703-036 HUMAN PRESCRIPTION DRUG Protopam Chloride pralidoxime chloride INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS 20240429 N/A NDA NDA014134 Bamboo US BidCo LLC PRALIDOXIME CHLORIDE 1 g/20mL 6 VIAL, SINGLE-DOSE in 1 PACKAGE (83703-036-01) / 20 mL in 1 VIAL, SINGLE-DOSE (83703-036-27)
60977-141-01 60977-141 HUMAN PRESCRIPTION DRUG Protopam Chloride pralidoxime chloride INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS 19650310 N/A NDA NDA014134 Baxter Healthcare Corporation PRALIDOXIME CHLORIDE 1 g/20mL 6 VIAL, SINGLE-DOSE in 1 PACKAGE (60977-141-01) / 20 mL in 1 VIAL, SINGLE-DOSE (60977-141-27)
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