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=ANDA211920"
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
68083-338-10 68083-338 HUMAN PRESCRIPTION DRUG phenylephrine hydrochloride phenylephrine hydrochloride INJECTION INTRAVENOUS 20201021 N/A ANDA ANDA211920 Gland Pharma Limited PHENYLEPHRINE HYDROCHLORIDE 10 mg/mL 10 VIAL in 1 CARTON (68083-338-10) / 5 mL in 1 VIAL (68083-338-01)
68083-339-01 68083-339 HUMAN PRESCRIPTION DRUG phenylephrine hydrochloride phenylephrine hydrochloride INJECTION INTRAVENOUS 20201021 N/A ANDA ANDA211920 Gland Pharma Limited PHENYLEPHRINE HYDROCHLORIDE 10 mg/mL 1 VIAL in 1 CARTON (68083-339-01) / 10 mL in 1 VIAL
68083-465-25 68083-465 HUMAN PRESCRIPTION DRUG Phenylephrine Hydrochloride Phenylephrine Hydrochloride Phenylephrine Hydrochloride INJECTION INTRAVENOUS 20210414 N/A ANDA ANDA211920 Gland Pharma Limited PHENYLEPHRINE HYDROCHLORIDE 10 mg/mL 25 VIAL in 1 CARTON (68083-465-25) / 1 mL in 1 VIAL (68083-465-01)
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