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=NDA019892"
符合检索条件的记录共 57 条，共 3 页，当前第 2 页 ，可点击列名称排序
首页 上一页 下一页 最后一页
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
87063-037-20 87063-037 HUMAN PRESCRIPTION DRUG Hydromorphone Hydrochloride Hydromorphone Hydrochloride TABLET ORAL 20251204 N/A NDA AUTHORIZED GENERIC NDA019892 ASCLEMED USA INC. HYDROMORPHONE HYDROCHLORIDE 2 mg/1 20 TABLET in 1 BOTTLE, PLASTIC (87063-037-20)
87063-037-30 87063-037 HUMAN PRESCRIPTION DRUG Hydromorphone Hydrochloride Hydromorphone Hydrochloride TABLET ORAL 20251204 N/A NDA AUTHORIZED GENERIC NDA019892 ASCLEMED USA INC. HYDROMORPHONE HYDROCHLORIDE 2 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (87063-037-30)
87063-037-60 87063-037 HUMAN PRESCRIPTION DRUG Hydromorphone Hydrochloride Hydromorphone Hydrochloride TABLET ORAL 20251204 N/A NDA AUTHORIZED GENERIC NDA019892 ASCLEMED USA INC. HYDROMORPHONE HYDROCHLORIDE 2 mg/1 60 TABLET in 1 BOTTLE, PLASTIC (87063-037-60)
42858-234-01 42858-234 HUMAN PRESCRIPTION DRUG Dilaudid hydromorphone hydrochloride TABLET ORAL 20170515 N/A NDA NDA019892 Rhodes Pharmaceuticals L.P. HYDROMORPHONE HYDROCHLORIDE 4 mg/1 100 TABLET in 1 BOTTLE, PLASTIC (42858-234-01)
42858-234-50 42858-234 HUMAN PRESCRIPTION DRUG Dilaudid hydromorphone hydrochloride TABLET ORAL 20170515 N/A NDA NDA019892 Rhodes Pharmaceuticals L.P. HYDROMORPHONE HYDROCHLORIDE 4 mg/1 500 TABLET in 1 BOTTLE, PLASTIC (42858-234-50)
42858-338-01 42858-338 HUMAN PRESCRIPTION DRUG Dilaudid hydromorphone hydrochloride TABLET ORAL 20170515 N/A NDA NDA019892 Rhodes Pharmaceuticals L.P. HYDROMORPHONE HYDROCHLORIDE 8 mg/1 100 TABLET in 1 BOTTLE, PLASTIC (42858-338-01)
87063-038-01 87063-038 HUMAN PRESCRIPTION DRUG Hydromorphone Hydrochloride Hydromorphone Hydrochloride TABLET ORAL 20251204 N/A NDA AUTHORIZED GENERIC NDA019892 ASCLEMED USA INC. HYDROMORPHONE HYDROCHLORIDE 4 mg/1 100 TABLET in 1 BOTTLE, PLASTIC (87063-038-01)
87063-038-05 87063-038 HUMAN PRESCRIPTION DRUG Hydromorphone Hydrochloride Hydromorphone Hydrochloride TABLET ORAL 20251204 N/A NDA AUTHORIZED GENERIC NDA019892 ASCLEMED USA INC. HYDROMORPHONE HYDROCHLORIDE 4 mg/1 5 TABLET in 1 BOTTLE, PLASTIC (87063-038-05)
87063-038-07 87063-038 HUMAN PRESCRIPTION DRUG Hydromorphone Hydrochloride Hydromorphone Hydrochloride TABLET ORAL 20251204 N/A NDA AUTHORIZED GENERIC NDA019892 ASCLEMED USA INC. HYDROMORPHONE HYDROCHLORIDE 4 mg/1 7 TABLET in 1 BOTTLE, PLASTIC (87063-038-07)
87063-038-10 87063-038 HUMAN PRESCRIPTION DRUG Hydromorphone Hydrochloride Hydromorphone Hydrochloride TABLET ORAL 20251204 N/A NDA AUTHORIZED GENERIC NDA019892 ASCLEMED USA INC. HYDROMORPHONE HYDROCHLORIDE 4 mg/1 10 TABLET in 1 BOTTLE, PLASTIC (87063-038-10)
87063-038-14 87063-038 HUMAN PRESCRIPTION DRUG Hydromorphone Hydrochloride Hydromorphone Hydrochloride TABLET ORAL 20251204 N/A NDA AUTHORIZED GENERIC NDA019892 ASCLEMED USA INC. HYDROMORPHONE HYDROCHLORIDE 4 mg/1 14 TABLET in 1 BOTTLE, PLASTIC (87063-038-14)
87063-038-20 87063-038 HUMAN PRESCRIPTION DRUG Hydromorphone Hydrochloride Hydromorphone Hydrochloride TABLET ORAL 20251204 N/A NDA AUTHORIZED GENERIC NDA019892 ASCLEMED USA INC. HYDROMORPHONE HYDROCHLORIDE 4 mg/1 20 TABLET in 1 BOTTLE, PLASTIC (87063-038-20)
87063-038-30 87063-038 HUMAN PRESCRIPTION DRUG Hydromorphone Hydrochloride Hydromorphone Hydrochloride TABLET ORAL 20251204 N/A NDA AUTHORIZED GENERIC NDA019892 ASCLEMED USA INC. HYDROMORPHONE HYDROCHLORIDE 4 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (87063-038-30)
87063-037-90 87063-037 HUMAN PRESCRIPTION DRUG Hydromorphone Hydrochloride Hydromorphone Hydrochloride TABLET ORAL 20251204 N/A NDA AUTHORIZED GENERIC NDA019892 ASCLEMED USA INC. HYDROMORPHONE HYDROCHLORIDE 2 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (87063-037-90)
42858-301-01 42858-301 HUMAN PRESCRIPTION DRUG Hydromorphone Hydrochloride Hydromorphone Hydrochloride TABLET ORAL 20091123 N/A NDA AUTHORIZED GENERIC NDA019892 Rhodes Pharmaceuticals L.P. HYDROMORPHONE HYDROCHLORIDE 2 mg/1 100 TABLET in 1 BOTTLE, PLASTIC (42858-301-01)
42858-301-25 42858-301 HUMAN PRESCRIPTION DRUG Hydromorphone Hydrochloride Hydromorphone Hydrochloride TABLET ORAL 20091123 N/A NDA AUTHORIZED GENERIC NDA019892 Rhodes Pharmaceuticals L.P. HYDROMORPHONE HYDROCHLORIDE 2 mg/1 4 BLISTER PACK in 1 CARTON (42858-301-25) / 25 TABLET in 1 BLISTER PACK
87063-039-01 87063-039 HUMAN PRESCRIPTION DRUG Hydromorphone Hydrochloride Hydromorphone Hydrochloride TABLET ORAL 20251204 N/A NDA AUTHORIZED GENERIC NDA019892 ASCLEMED USA INC. HYDROMORPHONE HYDROCHLORIDE 8 mg/1 100 TABLET in 1 BOTTLE, PLASTIC (87063-039-01)
87063-039-05 87063-039 HUMAN PRESCRIPTION DRUG Hydromorphone Hydrochloride Hydromorphone Hydrochloride TABLET ORAL 20251204 N/A NDA AUTHORIZED GENERIC NDA019892 ASCLEMED USA INC. HYDROMORPHONE HYDROCHLORIDE 8 mg/1 5 TABLET in 1 BOTTLE, PLASTIC (87063-039-05)
87063-039-07 87063-039 HUMAN PRESCRIPTION DRUG Hydromorphone Hydrochloride Hydromorphone Hydrochloride TABLET ORAL 20251204 N/A NDA AUTHORIZED GENERIC NDA019892 ASCLEMED USA INC. HYDROMORPHONE HYDROCHLORIDE 8 mg/1 7 TABLET in 1 BOTTLE, PLASTIC (87063-039-07)
87063-039-10 87063-039 HUMAN PRESCRIPTION DRUG Hydromorphone Hydrochloride Hydromorphone Hydrochloride TABLET ORAL 20251204 N/A NDA AUTHORIZED GENERIC NDA019892 ASCLEMED USA INC. HYDROMORPHONE HYDROCHLORIDE 8 mg/1 10 TABLET in 1 BOTTLE, PLASTIC (87063-039-10)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase