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=ANDA201633"
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
62756-969-64 62756-969 HUMAN PRESCRIPTION DRUG Buprenorphine and Naloxone Buprenorphine and Naloxone TABLET SUBLINGUAL 20170718 N/A ANDA ANDA201633 Sun Pharmaceutical Industries, Inc. BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE DIHYDRATE 2 mg/1; .5 mg/1 3 BLISTER PACK in 1 CARTON (62756-969-64) / 10 TABLET in 1 BLISTER PACK
62756-969-83 62756-969 HUMAN PRESCRIPTION DRUG Buprenorphine and Naloxone Buprenorphine and Naloxone TABLET SUBLINGUAL 20170718 N/A ANDA ANDA201633 Sun Pharmaceutical Industries, Inc. BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE DIHYDRATE 2 mg/1; .5 mg/1 30 TABLET in 1 BOTTLE (62756-969-83)
62756-970-64 62756-970 HUMAN PRESCRIPTION DRUG Buprenorphine and Naloxone Buprenorphine and Naloxone TABLET SUBLINGUAL 20170718 N/A ANDA ANDA201633 Sun Pharmaceutical Industries, Inc. BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE DIHYDRATE 8 mg/1; 2 mg/1 3 BLISTER PACK in 1 CARTON (62756-970-64) / 10 TABLET in 1 BLISTER PACK
62756-970-83 62756-970 HUMAN PRESCRIPTION DRUG Buprenorphine and Naloxone Buprenorphine and Naloxone TABLET SUBLINGUAL 20170718 N/A ANDA ANDA201633 Sun Pharmaceutical Industries, Inc. BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE DIHYDRATE 8 mg/1; 2 mg/1 30 TABLET in 1 BOTTLE (62756-970-83)
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