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
46122-817-61 46122-817 HUMAN OTC DRUG GOOD NEIGHBOR PHARMACY MUCUS DM dextromethorphan hydrobromide, guaifenesin TABLET, EXTENDED RELEASE ORAL 20250912 N/A ANDA ANDA207602 Amerisource Bergen DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN 30 mg/1; 600 mg/1 1 BOTTLE in 1 CARTON (46122-817-61) / 20 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
68196-812-45 68196-812 HUMAN OTC DRUG members mark mucus relief dm dextromethorphan HBr, guaifenesin TABLET, EXTENDED RELEASE ORAL 20250403 N/A ANDA ANDA207602 Sam's West Inc DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN 60 mg/1; 1200 mg/1 1 BOTTLE in 1 CARTON (68196-812-45) / 56 TABLET, EXTENDED RELEASE in 1 BOTTLE
70000-0722-1 70000-0722 HUMAN OTC DRUG Leader Mucus Relief DM dextromethorphan hydrobromide, guaifenesin TABLET, EXTENDED RELEASE ORAL 20250308 N/A ANDA ANDA207602 Cardinal Health 110, LLC. dba Leader DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN 30 mg/1; 600 mg/1 1 BOTTLE in 1 CARTON (70000-0722-1) / 20 TABLET, EXTENDED RELEASE in 1 BOTTLE
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