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=ANDA212756"
符合检索条件的记录共 4 条，共 1 页，当前第 1 页 ，可点击列名称排序
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
67296-2096-3 67296-2096 HUMAN PRESCRIPTION DRUG Buprenorphine and Naloxone buprenorphine and naloxone FILM BUCCAL; SUBLINGUAL 20230829 N/A ANDA ANDA212756 RedPharm Drug BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE 12 mg/1; 3 mg/1 30 FILM in 1 BOTTLE (67296-2096-3)
67296-2096-9 67296-2096 HUMAN PRESCRIPTION DRUG Buprenorphine and Naloxone buprenorphine and naloxone FILM BUCCAL; SUBLINGUAL 20230829 N/A ANDA ANDA212756 RedPharm Drug BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE 12 mg/1; 3 mg/1 9 FILM in 1 BOTTLE (67296-2096-9)
50742-364-30 50742-364 HUMAN PRESCRIPTION DRUG Buprenorphine and Naloxone buprenorphine and naloxone FILM BUCCAL; SUBLINGUAL 20230829 N/A ANDA ANDA212756 INGENUS PHARMACEUTICALS, LLC BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE 8 mg/1; 2 mg/1 30 POUCH in 1 CARTON (50742-364-30) / 1 FILM in 1 POUCH (50742-364-01)
50742-365-30 50742-365 HUMAN PRESCRIPTION DRUG Buprenorphine and Naloxone buprenorphine and naloxone FILM BUCCAL; SUBLINGUAL 20230829 N/A ANDA ANDA212756 INGENUS PHARMACEUTICALS, LLC BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE 12 mg/1; 3 mg/1 30 POUCH in 1 CARTON (50742-365-30) / 1 FILM in 1 POUCH (50742-365-01)
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