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=ANDA078776"
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
68071-3611-5 68071-3611 HUMAN PRESCRIPTION DRUG Ondansetron Ondansetron Hydrochloride SOLUTION ORAL 20240619 N/A ANDA ANDA078776 NuCare Pharmaceuticals,Inc. ONDANSETRON HYDROCHLORIDE 4 mg/5mL 1 BOTTLE, PLASTIC in 1 CARTON (68071-3611-5) / 50 mL in 1 BOTTLE, PLASTIC
16714-671-02 16714-671 HUMAN PRESCRIPTION DRUG Ondansetron Ondansetron Hydrochloride SOLUTION ORAL 20071128 N/A ANDA ANDA078776 NorthStar Rx LLC ONDANSETRON HYDROCHLORIDE 4 mg/5mL 1 BOTTLE, PLASTIC in 1 CARTON (16714-671-02) / 50 mL in 1 BOTTLE, PLASTIC
65862-208-04 65862-208 HUMAN PRESCRIPTION DRUG Ondansetron Ondansetron Hydrochloride SOLUTION ORAL 20071128 N/A ANDA ANDA078776 Aurobindo Pharma Limited ONDANSETRON HYDROCHLORIDE 4 mg/5mL 1 BOTTLE, PLASTIC in 1 CARTON (65862-208-04) / 50 mL in 1 BOTTLE, PLASTIC
65862-208-50 65862-208 HUMAN PRESCRIPTION DRUG Ondansetron Ondansetron Hydrochloride SOLUTION ORAL 20071128 N/A ANDA ANDA078776 Aurobindo Pharma Limited ONDANSETRON HYDROCHLORIDE 4 mg/5mL 1 BOTTLE in 1 CARTON (65862-208-50) / 50 mL in 1 BOTTLE
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