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=ANDA076051"
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
36000-324-02 36000-324 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol Hydrochloride INJECTION, SOLUTION INTRAVENOUS 20210126 N/A ANDA ANDA076051 Baxter Healthcare Corporation LABETALOL HYDROCHLORIDE 5 mg/mL 1 VIAL in 1 CARTON (36000-324-02) / 40 mL in 1 VIAL (36000-324-01)
36000-322-02 36000-322 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol Hydrochloride INJECTION, SOLUTION INTRAVENOUS 20210126 N/A ANDA ANDA076051 Baxter Healthcare Corporation LABETALOL HYDROCHLORIDE 5 mg/mL 1 VIAL in 1 CARTON (36000-322-02) / 20 mL in 1 VIAL (36000-322-01)
36000-320-10 36000-320 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol Hydrochloride INJECTION, SOLUTION INTRAVENOUS 20210126 N/A ANDA ANDA076051 Baxter Healthcare Corporation LABETALOL HYDROCHLORIDE 5 mg/mL 10 VIAL in 1 CARTON (36000-320-10) / 4 mL in 1 VIAL (36000-320-01)
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