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=NDA020747"
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
0093-7870-65 0093-7870 HUMAN PRESCRIPTION DRUG Fentanyl Citrate Fentanyl Citrate LOZENGE ORAL; TRANSMUCOSAL 20151208 20260531 NDA AUTHORIZED GENERIC NDA020747 Teva Pharmaceuticals USA, Inc. FENTANYL CITRATE 1600 ug/1 30 BLISTER PACK in 1 CARTON (0093-7870-65) / 1 LOZENGE in 1 BLISTER PACK (0093-7870-19)
0093-7868-65 0093-7868 HUMAN PRESCRIPTION DRUG Fentanyl Citrate Fentanyl Citrate LOZENGE ORAL; TRANSMUCOSAL 20151208 20260831 NDA AUTHORIZED GENERIC NDA020747 Teva Pharmaceuticals USA, Inc. FENTANYL CITRATE 800 ug/1 30 BLISTER PACK in 1 CARTON (0093-7868-65) / 1 LOZENGE in 1 BLISTER PACK (0093-7868-19)
0093-7866-65 0093-7866 HUMAN PRESCRIPTION DRUG Fentanyl Citrate Fentanyl Citrate LOZENGE ORAL; TRANSMUCOSAL 20151208 20260831 NDA AUTHORIZED GENERIC NDA020747 Teva Pharmaceuticals USA, Inc. FENTANYL CITRATE 400 ug/1 30 BLISTER PACK in 1 CARTON (0093-7866-65) / 1 LOZENGE in 1 BLISTER PACK (0093-7866-19)
0093-7865-65 0093-7865 HUMAN PRESCRIPTION DRUG Fentanyl Citrate Fentanyl Citrate LOZENGE ORAL; TRANSMUCOSAL 20151208 20260531 NDA AUTHORIZED GENERIC NDA020747 Teva Pharmaceuticals USA, Inc. FENTANYL CITRATE 200 ug/1 30 BLISTER PACK in 1 CARTON (0093-7865-65) / 1 LOZENGE in 1 BLISTER PACK (0093-7865-19)
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