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
50090-1078-0 50090-1078 HUMAN OTC DRUG Mucinex DM Guaifenesin and Dextromethorphan Hydrobromide TABLET, EXTENDED RELEASE ORAL 20141128 N/A NDA NDA021620 A-S Medication Solutions DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN 30 mg/1; 600 mg/1 2 BLISTER PACK in 1 CARTON (50090-1078-0) / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
17856-0056-1 17856-0056 HUMAN OTC DRUG Mucinex DM Guaifenesin and Dextromethorphan Hydrobromide TABLET, EXTENDED RELEASE ORAL 20240508 N/A NDA NDA021620 ATLANTIC BIOLOGICALS CORP. DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN 30 mg/1; 600 mg/1 1 TABLET, EXTENDED RELEASE in 1 PACKAGE (17856-0056-1)
50090-1077-0 50090-1077 HUMAN OTC DRUG Mucinex DM Guaifenesin and Dextromethorphan Hydrobromide TABLET, EXTENDED RELEASE ORAL 20141128 N/A NDA NDA021620 A-S Medication Solutions DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN 30 mg/1; 600 mg/1 1 BLISTER PACK in 1 CARTON (50090-1077-0) / 20 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
67751-171-01 67751-171 HUMAN OTC DRUG Mucinex DM DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN TABLET, EXTENDED RELEASE ORAL 20160923 N/A NDA NDA021620 Navajo Manufacturing Company Inc. DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN 30 mg/1; 600 mg/1 1 POUCH in 1 CARTON (67751-171-01) / 2 TABLET, EXTENDED RELEASE in 1 POUCH
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