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=ANDA203662"
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
0143-9318-10 0143-9318 HUMAN PRESCRIPTION DRUG Norepinephrine Bitartrate Norepinephrine Bitartrate INJECTION INTRAVENOUS 20180801 N/A ANDA ANDA203662 Hikma Pharmaceuticals USA Inc. NOREPINEPHRINE BITARTRATE 1 mg/mL 10 VIAL in 1 CARTON (0143-9318-10) / 4 mL in 1 VIAL (0143-9318-01)
51662-1528-1 51662-1528 HUMAN PRESCRIPTION DRUG NOREPINEPHRINE BITARTRATE NOREPINEPHRINE BITARTRATE INJECTION INTRAVENOUS 20210808 N/A ANDA ANDA203662 HF Acquisition Co LLC, DBA HealthFirst NOREPINEPHRINE BITARTRATE 1 mg/mL 4 mL in 1 VIAL (51662-1528-1)
51662-1528-3 51662-1528 HUMAN PRESCRIPTION DRUG NOREPINEPHRINE BITARTRATE NOREPINEPHRINE BITARTRATE INJECTION INTRAVENOUS 20220710 N/A ANDA ANDA203662 HF Acquisition Co LLC, DBA HealthFirst NOREPINEPHRINE BITARTRATE 1 mg/mL 10 POUCH in 1 CASE (51662-1528-3) / 1 VIAL in 1 POUCH (51662-1528-2) / 4 mL in 1 VIAL
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