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=ANDA207510"
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
87063-032-10 87063-032 HUMAN PRESCRIPTION DRUG OXYCODONE AND ACETAMINOPHEN oxycodone and acetaminophen TABLET ORAL 20251125 N/A ANDA ANDA207510 Asclemed USA, Inc. ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 5 mg/1 10 TABLET in 1 BOTTLE (87063-032-10)
87063-032-20 87063-032 HUMAN PRESCRIPTION DRUG OXYCODONE AND ACETAMINOPHEN oxycodone and acetaminophen TABLET ORAL 20251125 N/A ANDA ANDA207510 Asclemed USA, Inc. ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 5 mg/1 20 TABLET in 1 BOTTLE (87063-032-20)
87063-032-30 87063-032 HUMAN PRESCRIPTION DRUG OXYCODONE AND ACETAMINOPHEN oxycodone and acetaminophen TABLET ORAL 20251125 N/A ANDA ANDA207510 Asclemed USA, Inc. ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 5 mg/1 30 TABLET in 1 BOTTLE (87063-032-30)
87063-032-60 87063-032 HUMAN PRESCRIPTION DRUG OXYCODONE AND ACETAMINOPHEN oxycodone and acetaminophen TABLET ORAL 20251125 N/A ANDA ANDA207510 Asclemed USA, Inc. ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 5 mg/1 60 TABLET in 1 BOTTLE (87063-032-60)
87063-032-90 87063-032 HUMAN PRESCRIPTION DRUG OXYCODONE AND ACETAMINOPHEN oxycodone and acetaminophen TABLET ORAL 20251125 N/A ANDA ANDA207510 Asclemed USA, Inc. ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 5 mg/1 90 TABLET in 1 BOTTLE (87063-032-90)
87063-033-05 87063-033 HUMAN PRESCRIPTION DRUG OXYCODONE AND ACETAMINOPHEN oxycodone and acetaminophen TABLET ORAL 20251125 N/A ANDA ANDA207510 Asclemed USA, Inc. ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 7.5 mg/1 500 TABLET in 1 BOTTLE (87063-033-05)
87063-033-10 87063-033 HUMAN PRESCRIPTION DRUG OXYCODONE AND ACETAMINOPHEN oxycodone and acetaminophen TABLET ORAL 20251125 N/A ANDA ANDA207510 Asclemed USA, Inc. ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 7.5 mg/1 10 TABLET in 1 BOTTLE (87063-033-10)
71335-2049-1 71335-2049 HUMAN PRESCRIPTION DRUG OXYCODONE AND ACETAMINOPHEN oxycodone and acetaminophen TABLET ORAL 20220228 N/A ANDA ANDA207510 Bryant Ranch Prepack ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 10 mg/1 30 TABLET in 1 BOTTLE (71335-2049-1)
71335-2049-2 71335-2049 HUMAN PRESCRIPTION DRUG OXYCODONE AND ACETAMINOPHEN oxycodone and acetaminophen TABLET ORAL 20220228 N/A ANDA ANDA207510 Bryant Ranch Prepack ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 10 mg/1 120 TABLET in 1 BOTTLE (71335-2049-2)
71335-2049-3 71335-2049 HUMAN PRESCRIPTION DRUG OXYCODONE AND ACETAMINOPHEN oxycodone and acetaminophen TABLET ORAL 20220228 N/A ANDA ANDA207510 Bryant Ranch Prepack ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 10 mg/1 90 TABLET in 1 BOTTLE (71335-2049-3)
71335-2049-4 71335-2049 HUMAN PRESCRIPTION DRUG OXYCODONE AND ACETAMINOPHEN oxycodone and acetaminophen TABLET ORAL 20220228 N/A ANDA ANDA207510 Bryant Ranch Prepack ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 10 mg/1 28 TABLET in 1 BOTTLE (71335-2049-4)
71335-2049-5 71335-2049 HUMAN PRESCRIPTION DRUG OXYCODONE AND ACETAMINOPHEN oxycodone and acetaminophen TABLET ORAL 20220228 N/A ANDA ANDA207510 Bryant Ranch Prepack ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 10 mg/1 60 TABLET in 1 BOTTLE (71335-2049-5)
71335-2049-6 71335-2049 HUMAN PRESCRIPTION DRUG OXYCODONE AND ACETAMINOPHEN oxycodone and acetaminophen TABLET ORAL 20220228 N/A ANDA ANDA207510 Bryant Ranch Prepack ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 10 mg/1 20 TABLET in 1 BOTTLE (71335-2049-6)
71335-2049-7 71335-2049 HUMAN PRESCRIPTION DRUG OXYCODONE AND ACETAMINOPHEN oxycodone and acetaminophen TABLET ORAL 20220228 N/A ANDA ANDA207510 Bryant Ranch Prepack ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 10 mg/1 45 TABLET in 1 BOTTLE (71335-2049-7)
71335-2049-8 71335-2049 HUMAN PRESCRIPTION DRUG OXYCODONE AND ACETAMINOPHEN oxycodone and acetaminophen TABLET ORAL 20220228 N/A ANDA ANDA207510 Bryant Ranch Prepack ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 10 mg/1 75 TABLET in 1 BOTTLE (71335-2049-8)
71335-2049-9 71335-2049 HUMAN PRESCRIPTION DRUG OXYCODONE AND ACETAMINOPHEN oxycodone and acetaminophen TABLET ORAL 20220228 N/A ANDA ANDA207510 Bryant Ranch Prepack ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 10 mg/1 100 TABLET in 1 BOTTLE (71335-2049-9)
71930-047-12 71930-047 HUMAN PRESCRIPTION DRUG OXYCODONE AND ACETAMINOPHEN oxycodone and acetaminophen TABLET ORAL 20190601 N/A ANDA ANDA207510 Eywa Pharma Inc ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 10 mg/1 100 TABLET in 1 BOTTLE (71930-047-12)
71930-047-52 71930-047 HUMAN PRESCRIPTION DRUG OXYCODONE AND ACETAMINOPHEN oxycodone and acetaminophen TABLET ORAL 20190601 N/A ANDA ANDA207510 Eywa Pharma Inc ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 10 mg/1 500 TABLET in 1 BOTTLE (71930-047-52)
0904-7095-61 0904-7095 HUMAN PRESCRIPTION DRUG OXYCODONE AND ACETAMINOPHEN oxycodone and acetaminophen TABLET ORAL 20190601 N/A ANDA ANDA207510 Major Pharmaceuticals ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 10 mg/1 100 BLISTER PACK in 1 CARTON (0904-7095-61) / 1 TABLET in 1 BLISTER PACK
87063-033-20 87063-033 HUMAN PRESCRIPTION DRUG OXYCODONE AND ACETAMINOPHEN oxycodone and acetaminophen TABLET ORAL 20251125 N/A ANDA ANDA207510 Asclemed USA, Inc. ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 7.5 mg/1 20 TABLET in 1 BOTTLE (87063-033-20)
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