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=ANDA203894"
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
70518-3164-1 70518-3164 HUMAN PRESCRIPTION DRUG metoprolol succinate metoprolol succinate TABLET, EXTENDED RELEASE ORAL 20211005 N/A ANDA ANDA203894 REMEDYREPACK INC. METOPROLOL SUCCINATE 50 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-3164-1)
63739-097-10 63739-097 HUMAN PRESCRIPTION DRUG metoprolol succinate metoprolol succinate TABLET, EXTENDED RELEASE ORAL 20231130 N/A ANDA ANDA203894 McKesson Corporation DBA SKY Packaging METOPROLOL SUCCINATE 50 mg/1 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-097-10) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
70518-3122-0 70518-3122 HUMAN PRESCRIPTION DRUG metoprolol succinate metoprolol succinate TABLET, EXTENDED RELEASE ORAL 20210615 N/A ANDA ANDA203894 REMEDYREPACK INC. METOPROLOL SUCCINATE 100 mg/1 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-3122-0)
68071-2930-3 68071-2930 HUMAN PRESCRIPTION DRUG Metoprolol Succinate Metoprolol Succinate TABLET, EXTENDED RELEASE ORAL 20230206 N/A ANDA ANDA203894 NuCare Pharmaceuticals,Inc. METOPROLOL SUCCINATE 25 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-2930-3)
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