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=ANDA207419"
符合检索条件的记录共 122 条，共 7 页，当前第 6 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
72865-114-01 72865-114 HUMAN PRESCRIPTION DRUG OXYCODONE AND ACETAMINOPHEN Oxycodone and Acetaminophen TABLET ORAL 20190315 N/A ANDA ANDA207419 XLCare Pharmaceuticals, Inc. ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 5 mg/1 100 TABLET in 1 BOTTLE (72865-114-01)
72865-114-05 72865-114 HUMAN PRESCRIPTION DRUG OXYCODONE AND ACETAMINOPHEN Oxycodone and Acetaminophen TABLET ORAL 20190315 N/A ANDA ANDA207419 XLCare Pharmaceuticals, Inc. ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 5 mg/1 500 TABLET in 1 BOTTLE (72865-114-05)
72865-115-01 72865-115 HUMAN PRESCRIPTION DRUG OXYCODONE AND ACETAMINOPHEN Oxycodone and Acetaminophen TABLET ORAL 20190315 N/A ANDA ANDA207419 XLCare Pharmaceuticals, Inc. ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 7.5 mg/1 100 TABLET in 1 BOTTLE (72865-115-01)
72865-115-05 72865-115 HUMAN PRESCRIPTION DRUG OXYCODONE AND ACETAMINOPHEN Oxycodone and Acetaminophen TABLET ORAL 20190315 N/A ANDA ANDA207419 XLCare Pharmaceuticals, Inc. ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 7.5 mg/1 500 TABLET in 1 BOTTLE (72865-115-05)
72865-116-01 72865-116 HUMAN PRESCRIPTION DRUG OXYCODONE AND ACETAMINOPHEN Oxycodone and Acetaminophen TABLET ORAL 20190315 N/A ANDA ANDA207419 XLCare Pharmaceuticals, Inc. ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 10 mg/1 100 TABLET in 1 BOTTLE (72865-116-01)
72865-116-05 72865-116 HUMAN PRESCRIPTION DRUG OXYCODONE AND ACETAMINOPHEN Oxycodone and Acetaminophen TABLET ORAL 20190315 N/A ANDA ANDA207419 XLCare Pharmaceuticals, Inc. ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 10 mg/1 500 TABLET in 1 BOTTLE (72865-116-05)
72189-368-30 72189-368 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone and Acetaminophen TABLET ORAL 20220728 N/A ANDA ANDA207419 Direct_Rx ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 7.5 mg/1 30 TABLET in 1 BOTTLE (72189-368-30)
72189-368-60 72189-368 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone and Acetaminophen TABLET ORAL 20220728 N/A ANDA ANDA207419 Direct_Rx ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 7.5 mg/1 60 TABLET in 1 BOTTLE (72189-368-60)
72189-368-72 72189-368 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone and Acetaminophen TABLET ORAL 20220728 N/A ANDA ANDA207419 Direct_Rx ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 7.5 mg/1 120 TABLET in 1 BOTTLE (72189-368-72)
72189-368-90 72189-368 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone and Acetaminophen TABLET ORAL 20220728 N/A ANDA ANDA207419 Direct_Rx ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 7.5 mg/1 90 TABLET in 1 BOTTLE (72189-368-90)
68071-5054-2 68071-5054 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone and Acetaminophen TABLET ORAL 20190912 N/A ANDA ANDA207419 NuCare Pharmaceuticals,Inc. ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 5 mg/1 12 TABLET in 1 BOTTLE (68071-5054-2)
68071-5054-4 68071-5054 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone and Acetaminophen TABLET ORAL 20190912 N/A ANDA ANDA207419 NuCare Pharmaceuticals,Inc. ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 5 mg/1 4 TABLET in 1 BOTTLE (68071-5054-4)
68071-5054-6 68071-5054 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone and Acetaminophen TABLET ORAL 20190912 N/A ANDA ANDA207419 NuCare Pharmaceuticals,Inc. ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 5 mg/1 6 TABLET in 1 BOTTLE (68071-5054-6)
31722-193-01 31722-193 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone and Acetaminophen TABLET ORAL 20170411 N/A ANDA ANDA207419 Camber Pharmaceuticals, Inc. ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 7.5 mg/1 100 TABLET in 1 BOTTLE (31722-193-01)
31722-193-05 31722-193 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone and Acetaminophen TABLET ORAL 20170411 N/A ANDA ANDA207419 Camber Pharmaceuticals, Inc. ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 7.5 mg/1 500 TABLET in 1 BOTTLE (31722-193-05)
31722-192-01 31722-192 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone and Acetaminophen TABLET ORAL 20170411 N/A ANDA ANDA207419 Camber Pharmaceuticals, Inc. ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 5 mg/1 100 TABLET in 1 BOTTLE (31722-192-01)
31722-192-05 31722-192 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone and Acetaminophen TABLET ORAL 20170411 N/A ANDA ANDA207419 Camber Pharmaceuticals, Inc. ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 5 mg/1 500 TABLET in 1 BOTTLE (31722-192-05)
31722-191-01 31722-191 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone and Acetaminophen TABLET ORAL 20170411 N/A ANDA ANDA207419 Camber Pharmaceuticals, Inc. ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 2.5 mg/1 100 TABLET in 1 BOTTLE (31722-191-01)
31722-191-05 31722-191 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone and Acetaminophen TABLET ORAL 20170411 N/A ANDA ANDA207419 Camber Pharmaceuticals, Inc. ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 2.5 mg/1 500 TABLET in 1 BOTTLE (31722-191-05)
31722-948-05 31722-948 HUMAN PRESCRIPTION DRUG OXYCODONE AND ACETAMINOPHEN Oxycodone and Acetaminophen TABLET ORAL 20190315 N/A ANDA ANDA207419 Camber Pharmaceuticals, Inc. ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 2.5 mg/1 500 TABLET in 1 BOTTLE (31722-948-05)
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