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)
产品NDC42023-216
产品类型HUMAN PRESCRIPTION DRUG
商品名Ephedrine Sulfate
通用名Ephedrine Sulfate
剂型INJECTION, SOLUTION
给药途径INTRAVENOUS
市场类别NDA
申请号NDA208943
标签持有者Par Pharmaceutical, Inc.
活性成分EPHEDRINE SULFATE
规格50 mg/mL
药学分类Adrenergic alpha-Agonists [MoA], Adrenergic beta-Agonists [MoA], Increased Norepinephrine Activity [PE], Norepinephrine Releasing Agent [EPC], alpha-Adrenergic Agonist [EPC], beta-Adrenergic Agonist [EPC]
DEA计划编号N/A
上市认证有效期20241231
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产品NDCNDC包装代码包装描述开始上市日期结束上市日期NDC号状态是否样品包装药品说明书
42023-21642023-216-2525 VIAL in 1 CARTON (42023-216-25) / 1 mL in 1 VIAL (42023-216-01) 20170216有效药品说明书及标签信息
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