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=ANDA213203"
符合检索条件的记录共 10 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
79481-1002-1 79481-1002 HUMAN OTC DRUG Guaifenesin and Pseudoephedrine HCl Guaifenesin and Pseudoephedrine HCl TABLET, EXTENDED RELEASE ORAL 20210715 N/A ANDA ANDA213203 Meijer GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE 600 mg/1; 60 mg/1 1 BLISTER PACK in 1 CARTON (79481-1002-1) / 18 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
0363-0134-78 0363-0134 HUMAN OTC DRUG Guaifenesin and Pseudoephedrine HCl Guaifenesin and Pseudoephedrine HCl TABLET, EXTENDED RELEASE ORAL 20200805 N/A ANDA ANDA213203 WALGREEN CO. GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE 1200 mg/1; 120 mg/1 2 BLISTER PACK in 1 CARTON (0363-0134-78) / 12 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
30142-137-12 30142-137 HUMAN OTC DRUG Guaifenesin and Pseudoephedrine HCl Guaifenesin and Pseudoephedrine HCl TABLET, EXTENDED RELEASE ORAL 20210416 N/A ANDA ANDA213203 KROGER COMPANY GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE 600 mg/1; 60 mg/1 1 BLISTER PACK in 1 CARTON (30142-137-12) / 18 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
30142-137-17 30142-137 HUMAN OTC DRUG Guaifenesin and Pseudoephedrine HCl Guaifenesin and Pseudoephedrine HCl TABLET, EXTENDED RELEASE ORAL 20210416 N/A ANDA ANDA213203 KROGER COMPANY GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE 600 mg/1; 60 mg/1 2 BLISTER PACK in 1 CARTON (30142-137-17) / 18 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
0363-9946-40 0363-9946 HUMAN OTC DRUG Guaifenesin and Pseudoephedrine HCl Guaifenesin and Pseudoephedrine HCl TABLET, EXTENDED RELEASE ORAL 20220507 N/A ANDA ANDA213203 WALGREEN CO. GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE 600 mg/1; 60 mg/1 1 BLISTER PACK in 1 CARTON (0363-9946-40) / 18 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
0363-9946-45 0363-9946 HUMAN OTC DRUG Guaifenesin and Pseudoephedrine HCl Guaifenesin and Pseudoephedrine HCl TABLET, EXTENDED RELEASE ORAL 20220507 N/A ANDA ANDA213203 WALGREEN CO. GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE 600 mg/1; 60 mg/1 2 BLISTER PACK in 1 CARTON (0363-9946-45) / 18 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
58602-833-12 58602-833 HUMAN OTC DRUG Guaifenesin and Pseudoephedrine HCl Guaifenesin and Pseudoephedrine HCl TABLET, EXTENDED RELEASE ORAL 20200325 N/A ANDA ANDA213203 Aurohealth LLC GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE 600 mg/1; 60 mg/1 1 BLISTER PACK in 1 CARTON (58602-833-12) / 18 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
58602-833-17 58602-833 HUMAN OTC DRUG Guaifenesin and Pseudoephedrine HCl Guaifenesin and Pseudoephedrine HCl TABLET, EXTENDED RELEASE ORAL 20200325 N/A ANDA ANDA213203 Aurohealth LLC GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE 600 mg/1; 60 mg/1 2 BLISTER PACK in 1 CARTON (58602-833-17) / 18 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
58602-834-77 58602-834 HUMAN OTC DRUG Guaifenesin and Pseudoephedrine HCl Guaifenesin and Pseudoephedrine HCl TABLET, EXTENDED RELEASE ORAL 20200325 N/A ANDA ANDA213203 Aurohealth LLC GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE 1200 mg/1; 120 mg/1 1 BLISTER PACK in 1 CARTON (58602-834-77) / 12 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
58602-834-78 58602-834 HUMAN OTC DRUG Guaifenesin and Pseudoephedrine HCl Guaifenesin and Pseudoephedrine HCl TABLET, EXTENDED RELEASE ORAL 20200325 N/A ANDA ANDA213203 Aurohealth LLC GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE 1200 mg/1; 120 mg/1 2 BLISTER PACK in 1 CARTON (58602-834-78) / 12 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase