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=NDA217338"
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
72854-001-16 72854-001 HUMAN OTC DRUG Mucinex 12HR Cold and Fever Multi-Symptom Naproxen Sodium, Dextromethorphan Hydrobromide, Guaifenesin TABLET, EXTENDED RELEASE ORAL 20260601 N/A NDA NDA217338 Reckitt Benckiser LLC DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; NAPROXEN SODIUM 30 mg/1; 600 mg/1; 110 mg/1 2 BLISTER PACK in 1 CARTON (72854-001-16) / 8 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
72854-001-32 72854-001 HUMAN OTC DRUG Mucinex 12HR Cold and Fever Multi-Symptom Naproxen Sodium, Dextromethorphan Hydrobromide, Guaifenesin TABLET, EXTENDED RELEASE ORAL 20260601 N/A NDA NDA217338 Reckitt Benckiser LLC DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; NAPROXEN SODIUM 30 mg/1; 600 mg/1; 110 mg/1 4 BLISTER PACK in 1 CARTON (72854-001-32) / 8 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
72854-001-50 72854-001 HUMAN OTC DRUG Mucinex 12HR Cold and Fever Multi-Symptom Naproxen Sodium, Dextromethorphan Hydrobromide, Guaifenesin TABLET, EXTENDED RELEASE ORAL 20260601 N/A NDA NDA217338 Reckitt Benckiser LLC DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; NAPROXEN SODIUM 30 mg/1; 600 mg/1; 110 mg/1 5 BLISTER PACK in 1 CARTON (72854-001-50) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
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