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 58 条，共 3 页，当前第 1 页 ，可点击列名称排序
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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
71335-9701-0 71335-9701 HUMAN PRESCRIPTION DRUG Hydromorphone Hydrochloride Hydromorphone Hydrochloride TABLET ORAL 20250226 N/A NDA AUTHORIZED GENERIC NDA019892 Bryant Ranch Prepack HYDROMORPHONE HYDROCHLORIDE 4 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (71335-9701-0)
71335-9701-1 71335-9701 HUMAN PRESCRIPTION DRUG Hydromorphone Hydrochloride Hydromorphone Hydrochloride TABLET ORAL 20260112 N/A NDA AUTHORIZED GENERIC NDA019892 Bryant Ranch Prepack HYDROMORPHONE HYDROCHLORIDE 4 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (71335-9701-1)
71335-9701-2 71335-9701 HUMAN PRESCRIPTION DRUG Hydromorphone Hydrochloride Hydromorphone Hydrochloride TABLET ORAL 20260410 N/A NDA AUTHORIZED GENERIC NDA019892 Bryant Ranch Prepack HYDROMORPHONE HYDROCHLORIDE 4 mg/1 180 TABLET in 1 BOTTLE, PLASTIC (71335-9701-2)
71335-9701-3 71335-9701 HUMAN PRESCRIPTION DRUG Hydromorphone Hydrochloride Hydromorphone Hydrochloride TABLET ORAL 20260410 N/A NDA AUTHORIZED GENERIC NDA019892 Bryant Ranch Prepack HYDROMORPHONE HYDROCHLORIDE 4 mg/1 120 TABLET in 1 BOTTLE, PLASTIC (71335-9701-3)
71335-9701-4 71335-9701 HUMAN PRESCRIPTION DRUG Hydromorphone Hydrochloride Hydromorphone Hydrochloride TABLET ORAL 20260410 N/A NDA AUTHORIZED GENERIC NDA019892 Bryant Ranch Prepack HYDROMORPHONE HYDROCHLORIDE 4 mg/1 20 TABLET in 1 BOTTLE, PLASTIC (71335-9701-4)
71335-9701-5 71335-9701 HUMAN PRESCRIPTION DRUG Hydromorphone Hydrochloride Hydromorphone Hydrochloride TABLET ORAL 20260410 N/A NDA AUTHORIZED GENERIC NDA019892 Bryant Ranch Prepack HYDROMORPHONE HYDROCHLORIDE 4 mg/1 25 TABLET in 1 BOTTLE, PLASTIC (71335-9701-5)
71335-9701-6 71335-9701 HUMAN PRESCRIPTION DRUG Hydromorphone Hydrochloride Hydromorphone Hydrochloride TABLET ORAL 20260410 N/A NDA AUTHORIZED GENERIC NDA019892 Bryant Ranch Prepack HYDROMORPHONE HYDROCHLORIDE 4 mg/1 100 TABLET in 1 BOTTLE, PLASTIC (71335-9701-6)
71335-9701-7 71335-9701 HUMAN PRESCRIPTION DRUG Hydromorphone Hydrochloride Hydromorphone Hydrochloride TABLET ORAL 20240730 N/A NDA AUTHORIZED GENERIC NDA019892 Bryant Ranch Prepack HYDROMORPHONE HYDROCHLORIDE 4 mg/1 60 TABLET in 1 BOTTLE, PLASTIC (71335-9701-7)
71335-9701-8 71335-9701 HUMAN PRESCRIPTION DRUG Hydromorphone Hydrochloride Hydromorphone Hydrochloride TABLET ORAL 20260410 N/A NDA AUTHORIZED GENERIC NDA019892 Bryant Ranch Prepack HYDROMORPHONE HYDROCHLORIDE 4 mg/1 56 TABLET in 1 BOTTLE, PLASTIC (71335-9701-8)
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)
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)
87063-037-07 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)
87063-037-10 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 10 TABLET in 1 BOTTLE, PLASTIC (87063-037-10)
87063-037-14 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 14 TABLET in 1 BOTTLE, PLASTIC (87063-037-14)
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)
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 LLC 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 LLC HYDROMORPHONE HYDROCHLORIDE 2 mg/1 4 BLISTER PACK in 1 CARTON (42858-301-25) / 25 TABLET in 1 BLISTER PACK
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