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=ANDA207607"
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
67296-1877-3 67296-1877 HUMAN PRESCRIPTION DRUG Buprenorphine and Naloxone Buprenorphine and Naloxone FILM BUCCAL; SUBLINGUAL 20190220 N/A ANDA ANDA207607 Redpharm drug BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE DIHYDRATE 8 mg/1; 2 mg/1 30 FILM in 1 BOTTLE (67296-1877-3)
67296-1877-9 67296-1877 HUMAN PRESCRIPTION DRUG Buprenorphine and Naloxone Buprenorphine and Naloxone FILM BUCCAL; SUBLINGUAL 20190220 N/A ANDA ANDA207607 Redpharm drug BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE DIHYDRATE 8 mg/1; 2 mg/1 9 FILM in 1 BOTTLE (67296-1877-9)
0378-8767-93 0378-8767 HUMAN PRESCRIPTION DRUG Buprenorphine and Naloxone Buprenorphine and Naloxone FILM BUCCAL; SUBLINGUAL 20190220 N/A ANDA ANDA207607 Mylan Pharmaceuticals Inc. BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE DIHYDRATE 8 mg/1; 2 mg/1 30 POUCH in 1 CARTON (0378-8767-93) / 1 FILM in 1 POUCH (0378-8767-16)
0378-8768-93 0378-8768 HUMAN PRESCRIPTION DRUG Buprenorphine and Naloxone Buprenorphine and Naloxone FILM BUCCAL; SUBLINGUAL 20190220 N/A ANDA ANDA207607 Mylan Pharmaceuticals Inc. BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE DIHYDRATE 12 mg/1; 3 mg/1 30 POUCH in 1 CARTON (0378-8768-93) / 1 FILM in 1 POUCH (0378-8768-16)
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