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=ANDA205954"
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
47781-356-03 47781-356 HUMAN PRESCRIPTION DRUG Buprenorphine and Naloxone Sublingual Film Buprenorphine and Naloxone FILM BUCCAL; SUBLINGUAL 20190211 N/A ANDA ANDA205954 Alvogen Inc. BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE DIHYDRATE 4 mg/1; 1 mg/1 30 POUCH in 1 CARTON (47781-356-03) / 1 FILM in 1 POUCH (47781-356-11)
47781-357-03 47781-357 HUMAN PRESCRIPTION DRUG Buprenorphine and Naloxone Sublingual Film Buprenorphine and Naloxone FILM BUCCAL; SUBLINGUAL 20190211 N/A ANDA ANDA205954 Alvogen Inc. BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE DIHYDRATE 8 mg/1; 2 mg/1 30 POUCH in 1 CARTON (47781-357-03) / 1 FILM in 1 POUCH (47781-357-11)
47781-358-03 47781-358 HUMAN PRESCRIPTION DRUG Buprenorphine and Naloxone Sublingual Film Buprenorphine and Naloxone FILM BUCCAL; SUBLINGUAL 20190211 N/A ANDA ANDA205954 Alvogen Inc. BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE DIHYDRATE 12 mg/1; 3 mg/1 30 POUCH in 1 CARTON (47781-358-03) / 1 FILM in 1 POUCH (47781-358-11)
47781-355-03 47781-355 HUMAN PRESCRIPTION DRUG Buprenorphine and Naloxone Sublingual Film Buprenorphine and Naloxone FILM BUCCAL; SUBLINGUAL 20190211 N/A ANDA ANDA205954 Alvogen Inc. BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE DIHYDRATE 2 mg/1; .5 mg/1 30 POUCH in 1 CARTON (47781-355-03) / 1 FILM in 1 POUCH (47781-355-11)
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