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=NDA021585"
符合检索条件的记录共 9 条，共 1 页，当前第 1 页 ，可点击列名称排序
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
0363-0077-18 0363-0077 HUMAN OTC DRUG Guaifenesin and Pseudoephedrine Hydrochloride Guaifenesin and Pseudoephedrine Hydrochloride TABLET, EXTENDED RELEASE ORAL 20170801 N/A NDA NDA021585 WALGREEN COMPANY GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE 600 mg/1; 60 mg/1 1 BLISTER PACK in 1 CARTON (0363-0077-18) / 18 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
0363-0077-36 0363-0077 HUMAN OTC DRUG Guaifenesin and Pseudoephedrine Hydrochloride Guaifenesin and Pseudoephedrine Hydrochloride TABLET, EXTENDED RELEASE ORAL 20170801 N/A NDA NDA021585 WALGREEN COMPANY GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE 600 mg/1; 60 mg/1 2 BLISTER PACK in 1 CARTON (0363-0077-36) / 18 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
0536-1137-21 0536-1137 HUMAN OTC DRUG Mucus Relief D Guaifenesin and Pseudoephedrine Hydrochloride TABLET, EXTENDED RELEASE ORAL 20180301 N/A NDA NDA021585 Rugby Laboratories GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE 600 mg/1; 60 mg/1 1 BLISTER PACK in 1 CARTON (0536-1137-21) / 18 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
0536-1137-36 0536-1137 HUMAN OTC DRUG Mucus Relief D Guaifenesin and Pseudoephedrine Hydrochloride TABLET, EXTENDED RELEASE ORAL 20180301 N/A NDA NDA021585 Rugby Laboratories GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE 600 mg/1; 60 mg/1 2 BLISTER PACK in 1 CARTON (0536-1137-36) / 18 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
63824-057-18 63824-057 HUMAN OTC DRUG Mucinex D Guaifenesin and Pseudoephedrine Hydrochloride TABLET, EXTENDED RELEASE ORAL 20120626 N/A NDA NDA021585 RB Health (US) LLC GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE 600 mg/1; 60 mg/1 1 BLISTER PACK in 1 CARTON (63824-057-18) / 18 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
63824-057-36 63824-057 HUMAN OTC DRUG Mucinex D Guaifenesin and Pseudoephedrine Hydrochloride TABLET, EXTENDED RELEASE ORAL 20120626 N/A NDA NDA021585 RB Health (US) LLC GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE 600 mg/1; 60 mg/1 4 BLISTER PACK in 1 CARTON (63824-057-36) / 9 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
50090-1075-0 50090-1075 HUMAN OTC DRUG Mucinex D Guaifenesin and Pseudoephedrine Hydrochloride TABLET, EXTENDED RELEASE ORAL 20141128 N/A NDA NDA021585 A-S Medication Solutions GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE 600 mg/1; 60 mg/1 1 BLISTER PACK in 1 CARTON (50090-1075-0) / 18 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
63824-041-24 63824-041 HUMAN OTC DRUG Mucinex D Maximum Strength Guaifenesin and Pseudoephedrine Hydrochloride TABLET, EXTENDED RELEASE ORAL 20120626 N/A NDA NDA021585 RB Health (US) LLC GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE 1200 mg/1; 120 mg/1 2 BLISTER PACK in 1 CARTON (63824-041-24) / 12 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
50090-1076-0 50090-1076 HUMAN OTC DRUG MUCINEX D Guaifenesin and Pseudoephedrine Hydrochloride TABLET, EXTENDED RELEASE ORAL 20141128 N/A NDA NDA021585 A-S Medication Solutions GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE 600 mg/1; 60 mg/1 4 BLISTER PACK in 1 CARTON (50090-1076-0) / 9 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
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