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"
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
87063-039-14 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 14 TABLET in 1 BOTTLE, PLASTIC (87063-039-14)
87063-039-20 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 20 TABLET in 1 BOTTLE, PLASTIC (87063-039-20)
87063-039-30 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 30 TABLET in 1 BOTTLE, PLASTIC (87063-039-30)
87063-039-60 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 60 TABLET in 1 BOTTLE, PLASTIC (87063-039-60)
87063-039-90 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 90 TABLET in 1 BOTTLE, PLASTIC (87063-039-90)
87063-037-07 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 7 TABLET in 1 BOTTLE, PLASTIC (87063-037-07)
87063-037-05 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 5 TABLET in 1 BOTTLE, PLASTIC (87063-037-05)
87063-037-01 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/1 100 TABLET in 1 BOTTLE, PLASTIC (87063-037-01)
63629-4284-1 63629-4284 HUMAN PRESCRIPTION DRUG Hydromorphone Hydrochloride Hydromorphone Hydrochloride TABLET ORAL 20100621 N/A NDA AUTHORIZED GENERIC NDA019892 Bryant Ranch Prepack HYDROMORPHONE HYDROCHLORIDE 2 mg/1 25 TABLET in 1 BOTTLE (63629-4284-1)
63629-4284-5 63629-4284 HUMAN PRESCRIPTION DRUG Hydromorphone Hydrochloride Hydromorphone Hydrochloride TABLET ORAL 20140611 N/A NDA AUTHORIZED GENERIC NDA019892 Bryant Ranch Prepack HYDROMORPHONE HYDROCHLORIDE 2 mg/1 90 TABLET in 1 BOTTLE (63629-4284-5)
63629-4284-6 63629-4284 HUMAN PRESCRIPTION DRUG Hydromorphone Hydrochloride Hydromorphone Hydrochloride TABLET ORAL 20120625 N/A NDA AUTHORIZED GENERIC NDA019892 Bryant Ranch Prepack HYDROMORPHONE HYDROCHLORIDE 2 mg/1 120 TABLET in 1 BOTTLE (63629-4284-6)
63629-4284-7 63629-4284 HUMAN PRESCRIPTION DRUG Hydromorphone Hydrochloride Hydromorphone Hydrochloride TABLET ORAL 20140127 N/A NDA AUTHORIZED GENERIC NDA019892 Bryant Ranch Prepack HYDROMORPHONE HYDROCHLORIDE 2 mg/1 40 TABLET in 1 BOTTLE (63629-4284-7)
63629-4284-8 63629-4284 HUMAN PRESCRIPTION DRUG Hydromorphone Hydrochloride Hydromorphone Hydrochloride TABLET ORAL 20120501 N/A NDA AUTHORIZED GENERIC NDA019892 Bryant Ranch Prepack HYDROMORPHONE HYDROCHLORIDE 2 mg/1 20 TABLET in 1 BOTTLE (63629-4284-8)
63629-4284-9 63629-4284 HUMAN PRESCRIPTION DRUG Hydromorphone Hydrochloride Hydromorphone Hydrochloride TABLET ORAL 20200824 N/A NDA AUTHORIZED GENERIC NDA019892 Bryant Ranch Prepack HYDROMORPHONE HYDROCHLORIDE 2 mg/1 10 TABLET in 1 BOTTLE (63629-4284-9)
63629-4284-2 63629-4284 HUMAN PRESCRIPTION DRUG Hydromorphone Hydrochloride Hydromorphone Hydrochloride TABLET ORAL 20110823 N/A NDA AUTHORIZED GENERIC NDA019892 Bryant Ranch Prepack HYDROMORPHONE HYDROCHLORIDE 2 mg/1 60 TABLET in 1 BOTTLE (63629-4284-2)
63629-4284-3 63629-4284 HUMAN PRESCRIPTION DRUG Hydromorphone Hydrochloride Hydromorphone Hydrochloride TABLET ORAL 20101022 N/A NDA AUTHORIZED GENERIC NDA019892 Bryant Ranch Prepack HYDROMORPHONE HYDROCHLORIDE 2 mg/1 30 TABLET in 1 BOTTLE (63629-4284-3)
63629-4284-4 63629-4284 HUMAN PRESCRIPTION DRUG Hydromorphone Hydrochloride Hydromorphone Hydrochloride TABLET ORAL 20101112 N/A NDA AUTHORIZED GENERIC NDA019892 Bryant Ranch Prepack HYDROMORPHONE HYDROCHLORIDE 2 mg/1 28 TABLET in 1 BOTTLE (63629-4284-4)
42858-122-01 42858-122 HUMAN PRESCRIPTION DRUG Dilaudid hydromorphone hydrochloride TABLET ORAL 20170515 N/A NDA NDA019892 Rhodes Pharmaceuticals L.P. HYDROMORPHONE HYDROCHLORIDE 2 mg/1 100 TABLET in 1 BOTTLE, PLASTIC (42858-122-01)
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
42858-302-01 42858-302 HUMAN PRESCRIPTION DRUG Hydromorphone Hydrochloride Hydromorphone Hydrochloride TABLET ORAL 20091123 N/A NDA AUTHORIZED GENERIC NDA019892 Rhodes Pharmaceuticals L.P. HYDROMORPHONE HYDROCHLORIDE 4 mg/1 100 TABLET in 1 BOTTLE, PLASTIC (42858-302-01)
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