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=ANDA207602"
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
69842-812-55 69842-812 HUMAN OTC DRUG mucus dm extended release guaifenesin, dextromethorphan HBr TABLET, EXTENDED RELEASE ORAL 20180503 N/A ANDA ANDA207602 CVS Pharmacy DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN 60 mg/1; 1200 mg/1 1 BOTTLE in 1 CARTON (69842-812-55) / 42 TABLET, EXTENDED RELEASE in 1 BOTTLE
69842-812-66 69842-812 HUMAN OTC DRUG mucus dm extended release guaifenesin, dextromethorphan HBr TABLET, EXTENDED RELEASE ORAL 20180503 N/A ANDA ANDA207602 CVS Pharmacy DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN 60 mg/1; 1200 mg/1 1 BOTTLE in 1 CARTON (69842-812-66) / 14 TABLET, EXTENDED RELEASE in 1 BOTTLE
69842-812-30 69842-812 HUMAN OTC DRUG mucus dm extended release guaifenesin, dextromethorphan HBr TABLET, EXTENDED RELEASE ORAL 20180503 N/A ANDA ANDA207602 CVS Pharmacy DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN 60 mg/1; 1200 mg/1 1 BOTTLE in 1 CARTON (69842-812-30) / 28 TABLET, EXTENDED RELEASE in 1 BOTTLE
11673-235-30 11673-235 HUMAN OTC DRUG up and up maximum strength mucus relief dm dextromethorphan hydrobromide, guaifenesin TABLET, EXTENDED RELEASE ORAL 20180927 N/A ANDA ANDA207602 Target Corporation DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN 60 mg/1; 1200 mg/1 1 BOTTLE in 1 CARTON (11673-235-30) / 28 TABLET, EXTENDED RELEASE in 1 BOTTLE
11673-235-55 11673-235 HUMAN OTC DRUG up and up maximum strength mucus relief dm dextromethorphan hydrobromide, guaifenesin TABLET, EXTENDED RELEASE ORAL 20200417 N/A ANDA ANDA207602 Target Corporation DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN 60 mg/1; 1200 mg/1 1 BOTTLE in 1 CARTON (11673-235-55) / 42 TABLET, EXTENDED RELEASE in 1 BOTTLE
11673-235-66 11673-235 HUMAN OTC DRUG up and up maximum strength mucus relief dm dextromethorphan hydrobromide, guaifenesin TABLET, EXTENDED RELEASE ORAL 20180927 N/A ANDA ANDA207602 Target Corporation DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN 60 mg/1; 1200 mg/1 1 BOTTLE in 1 CARTON (11673-235-66) / 14 TABLET, EXTENDED RELEASE in 1 BOTTLE
11673-716-01 11673-716 HUMAN OTC DRUG up and up mucus relief dm dextromethorphan hydrobromide, guaifenesin TABLET, EXTENDED RELEASE ORAL 20190715 N/A ANDA ANDA207602 Target Corporation DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN 30 mg/1; 600 mg/1 1 BOTTLE in 1 CARTON (11673-716-01) / 20 TABLET, EXTENDED RELEASE in 1 BOTTLE
11673-716-49 11673-716 HUMAN OTC DRUG up and up mucus relief dm dextromethorphan hydrobromide, guaifenesin TABLET, EXTENDED RELEASE ORAL 20190715 N/A ANDA ANDA207602 Target Corporation DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN 30 mg/1; 600 mg/1 1 BOTTLE in 1 CARTON (11673-716-49) / 40 TABLET, EXTENDED RELEASE in 1 BOTTLE
36800-219-01 36800-219 HUMAN OTC DRUG Topcare Mucus DM dextromethorphan hydrobromide, guaifenesin TABLET, EXTENDED RELEASE ORAL 20190710 N/A ANDA ANDA207602 Topco Associates LLC DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN 30 mg/1; 600 mg/1 1 BOTTLE in 1 CARTON (36800-219-01) / 20 TABLET, EXTENDED RELEASE in 1 BOTTLE
36800-219-49 36800-219 HUMAN OTC DRUG Topcare Mucus DM dextromethorphan hydrobromide, guaifenesin TABLET, EXTENDED RELEASE ORAL 20220413 N/A ANDA ANDA207602 Topco Associates LLC DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN 30 mg/1; 600 mg/1 1 BOTTLE in 1 CARTON (36800-219-49) / 40 TABLET, EXTENDED RELEASE in 1 BOTTLE
37808-812-66 37808-812 HUMAN OTC DRUG mucus relief dm dextromethorphan HBr, guaifenesin TABLET, EXTENDED RELEASE ORAL 20180625 N/A ANDA ANDA207602 H E B DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN 60 mg/1; 1200 mg/1 1 BOTTLE in 1 CARTON (37808-812-66) / 14 TABLET, EXTENDED RELEASE in 1 BOTTLE
0363-6812-55 0363-6812 HUMAN OTC DRUG mucus relief dm dextromethorphan hydrobromide, guaifenesin TABLET, EXTENDED RELEASE ORAL 20181221 N/A ANDA ANDA207602 Walgreen Company DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN 60 mg/1; 1200 mg/1 1 BOTTLE in 1 CARTON (0363-6812-55) / 42 TABLET, EXTENDED RELEASE in 1 BOTTLE
0363-6812-66 0363-6812 HUMAN OTC DRUG mucus relief dm dextromethorphan hydrobromide, guaifenesin TABLET, EXTENDED RELEASE ORAL 20190107 N/A ANDA ANDA207602 Walgreen Company DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN 60 mg/1; 1200 mg/1 1 BOTTLE in 1 CARTON (0363-6812-66) / 14 TABLET, EXTENDED RELEASE in 1 BOTTLE
55301-812-66 55301-812 HUMAN OTC DRUG Exchange Select Mucus DM dextromethorphan HBr, guaifenesin TABLET, EXTENDED RELEASE ORAL 20180801 N/A ANDA ANDA207602 Army & Air Force Exchange Service DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN 60 mg/1; 1200 mg/1 1 BOTTLE in 1 CARTON (55301-812-66) / 14 TABLET, EXTENDED RELEASE in 1 BOTTLE
68391-812-01 68391-812 HUMAN OTC DRUG Berkley and Jensen Mucus Relief DM dextromethorphan HBr, guaifenesin TABLET, EXTENDED RELEASE ORAL 20250904 N/A ANDA ANDA207602 BJWC DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN 60 mg/1; 1200 mg/1 1 BOTTLE in 1 CARTON (68391-812-01) / 84 TABLET, EXTENDED RELEASE in 1 BOTTLE
68391-812-45 68391-812 HUMAN OTC DRUG Berkley and Jensen Mucus Relief DM dextromethorphan HBr, guaifenesin TABLET, EXTENDED RELEASE ORAL 20200715 N/A ANDA ANDA207602 BJWC DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN 60 mg/1; 1200 mg/1 1 BOTTLE in 1 CARTON (68391-812-45) / 56 TABLET, EXTENDED RELEASE in 1 BOTTLE
0363-6812-30 0363-6812 HUMAN OTC DRUG mucus relief dm dextromethorphan hydrobromide, guaifenesin TABLET, EXTENDED RELEASE ORAL 20190107 N/A ANDA ANDA207602 Walgreen Company DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN 60 mg/1; 1200 mg/1 1 BOTTLE in 1 CARTON (0363-6812-30) / 28 TABLET, EXTENDED RELEASE in 1 BOTTLE
41163-781-66 41163-781 HUMAN OTC DRUG Equaline Mucus DM dextromethorphan HBr, guaifenesin TABLET, EXTENDED RELEASE ORAL 20200224 N/A ANDA ANDA207602 United Natural Foods, Inc. dba UNFI DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN 60 mg/1; 1200 mg/1 1 BOTTLE in 1 CARTON (41163-781-66) / 14 TABLET, EXTENDED RELEASE in 1 BOTTLE
41163-599-01 41163-599 HUMAN OTC DRUG equaline mucus dm dextromethorphan hydrobromide, guaifenesin TABLET, EXTENDED RELEASE ORAL 20200218 N/A ANDA ANDA207602 United Natural Foods, Inc. dba UNFI DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN 30 mg/1; 600 mg/1 1 BOTTLE in 1 CARTON (41163-599-01) / 20 TABLET, EXTENDED RELEASE in 1 BOTTLE
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