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=NDA021620"
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
63824-072-46 63824-072 HUMAN OTC DRUG Mucinex DM Maximum Strength Guaifenesin and Dextromethorphan Hydrobromide TABLET, EXTENDED RELEASE ORAL 20120626 N/A NDA NDA021620 RB Health (US) LLC DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN 60 mg/1; 1200 mg/1 3 BLISTER PACK in 1 CARTON (63824-072-46) / 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
63824-072-48 63824-072 HUMAN OTC DRUG Mucinex DM Maximum Strength Guaifenesin and Dextromethorphan Hydrobromide TABLET, EXTENDED RELEASE ORAL 20120626 N/A NDA NDA021620 RB Health (US) LLC DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN 60 mg/1; 1200 mg/1 4 BLISTER PACK in 1 CARTON (63824-072-48) / 12 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
63824-072-56 63824-072 HUMAN OTC DRUG Mucinex DM Maximum Strength Guaifenesin and Dextromethorphan Hydrobromide TABLET, EXTENDED RELEASE ORAL 20210701 N/A NDA NDA021620 RB Health (US) LLC DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN 60 mg/1; 1200 mg/1 4 BLISTER PACK in 1 CARTON (63824-072-56) / 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
63824-056-74 63824-056 HUMAN OTC DRUG Mucinex DM Guaifenesin and Dextromethorphan Hydrobromide TABLET, EXTENDED RELEASE ORAL 20120626 N/A NDA NDA021620 RB Health (US) LLC DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN 30 mg/1; 600 mg/1 24 POUCH in 1 CARTON (63824-056-74) / 2 TABLET, EXTENDED RELEASE in 1 POUCH (63824-056-73)
63824-056-80 63824-056 HUMAN OTC DRUG Mucinex DM Guaifenesin and Dextromethorphan Hydrobromide TABLET, EXTENDED RELEASE ORAL 20240501 N/A NDA NDA021620 RB Health (US) LLC DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN 30 mg/1; 600 mg/1 2 BLISTER PACK in 1 CARTON (63824-056-80) / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
63824-056-89 63824-056 HUMAN OTC DRUG Mucinex DM Guaifenesin and Dextromethorphan Hydrobromide TABLET, EXTENDED RELEASE ORAL 20180330 N/A NDA NDA021620 RB Health (US) LLC DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN 30 mg/1; 600 mg/1 4 BLISTER PACK in 1 CARTON (63824-056-89) / 17 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
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