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=BLA761224"
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
55513-112-01 55513-112 HUMAN PRESCRIPTION DRUG TEZSPIRE tezepelumab-ekko INJECTION, SOLUTION SUBCUTANEOUS 20211217 N/A BLA BLA761224 Amgen, Inc TEZEPELUMAB 210 mg/1.9mL 1 SYRINGE in 1 CARTON (55513-112-01) / 1.91 mL in 1 SYRINGE
55513-112-96 55513-112 HUMAN PRESCRIPTION DRUG TEZSPIRE tezepelumab-ekko INJECTION, SOLUTION SUBCUTANEOUS 20211217 N/A BLA BLA761224 Amgen, Inc TEZEPELUMAB 210 mg/1.9mL 1 SYRINGE in 1 CARTON (55513-112-96) / 1.91 mL in 1 SYRINGE
55513-112-99 55513-112 HUMAN PRESCRIPTION DRUG TEZSPIRE tezepelumab-ekko INJECTION, SOLUTION SUBCUTANEOUS 20211217 N/A BLA BLA761224 Amgen, Inc TEZEPELUMAB 210 mg/1.9mL 1.91 mL in 1 SYRINGE (55513-112-99)
55513-100-01 55513-100 HUMAN PRESCRIPTION DRUG TEZSPIRE tezepelumab-ekko INJECTION, SOLUTION SUBCUTANEOUS 20211217 N/A BLA BLA761224 Amgen, Inc TEZEPELUMAB 210 mg/1.9mL 1 VIAL, GLASS in 1 CARTON (55513-100-01) / 1.91 mL in 1 VIAL, GLASS
55513-100-96 55513-100 HUMAN PRESCRIPTION DRUG TEZSPIRE tezepelumab-ekko INJECTION, SOLUTION SUBCUTANEOUS 20211217 N/A BLA BLA761224 Amgen, Inc TEZEPELUMAB 210 mg/1.9mL 1 VIAL, GLASS in 1 CARTON (55513-100-96) / 1.91 mL in 1 VIAL, GLASS
55513-100-99 55513-100 HUMAN PRESCRIPTION DRUG TEZSPIRE tezepelumab-ekko INJECTION, SOLUTION SUBCUTANEOUS 20211217 N/A BLA BLA761224 Amgen, Inc TEZEPELUMAB 210 mg/1.9mL 1.91 mL in 1 VIAL, GLASS (55513-100-99)
55513-123-01 55513-123 HUMAN PRESCRIPTION DRUG TEZSPIRE tezepelumab-ekko INJECTION, SOLUTION SUBCUTANEOUS 20230214 N/A BLA BLA761224 Amgen, Inc TEZEPELUMAB 210 mg/1.9mL 1 CARTRIDGE in 1 CARTON (55513-123-01) / 1.91 mL in 1 CARTRIDGE
55513-123-96 55513-123 HUMAN PRESCRIPTION DRUG TEZSPIRE tezepelumab-ekko INJECTION, SOLUTION SUBCUTANEOUS 20240220 N/A BLA BLA761224 Amgen, Inc TEZEPELUMAB 210 mg/1.9mL 1 CARTRIDGE in 1 CARTON (55513-123-96) / 1.91 mL in 1 CARTRIDGE
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