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"
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
71335-2106-1 71335-2106 HUMAN PRESCRIPTION DRUG OXYCODONE AND ACETAMINOPHEN Oxycodone and Acetaminophen TABLET ORAL 20220705 N/A ANDA ANDA207419 Bryant Ranch Prepack ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 10 mg/1 30 TABLET in 1 BOTTLE (71335-2106-1)
71335-2106-2 71335-2106 HUMAN PRESCRIPTION DRUG OXYCODONE AND ACETAMINOPHEN Oxycodone and Acetaminophen TABLET ORAL 20240531 N/A ANDA ANDA207419 Bryant Ranch Prepack ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 10 mg/1 120 TABLET in 1 BOTTLE (71335-2106-2)
71335-2106-3 71335-2106 HUMAN PRESCRIPTION DRUG OXYCODONE AND ACETAMINOPHEN Oxycodone and Acetaminophen TABLET ORAL 20220711 N/A ANDA ANDA207419 Bryant Ranch Prepack ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 10 mg/1 90 TABLET in 1 BOTTLE (71335-2106-3)
71335-2106-4 71335-2106 HUMAN PRESCRIPTION DRUG OXYCODONE AND ACETAMINOPHEN Oxycodone and Acetaminophen TABLET ORAL 20240531 N/A ANDA ANDA207419 Bryant Ranch Prepack ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 10 mg/1 28 TABLET in 1 BOTTLE (71335-2106-4)
71335-2106-5 71335-2106 HUMAN PRESCRIPTION DRUG OXYCODONE AND ACETAMINOPHEN Oxycodone and Acetaminophen TABLET ORAL 20220610 N/A ANDA ANDA207419 Bryant Ranch Prepack ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 10 mg/1 60 TABLET in 1 BOTTLE (71335-2106-5)
71335-2106-6 71335-2106 HUMAN PRESCRIPTION DRUG OXYCODONE AND ACETAMINOPHEN Oxycodone and Acetaminophen TABLET ORAL 20240531 N/A ANDA ANDA207419 Bryant Ranch Prepack ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 10 mg/1 20 TABLET in 1 BOTTLE (71335-2106-6)
71335-2106-7 71335-2106 HUMAN PRESCRIPTION DRUG OXYCODONE AND ACETAMINOPHEN Oxycodone and Acetaminophen TABLET ORAL 20240531 N/A ANDA ANDA207419 Bryant Ranch Prepack ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 10 mg/1 45 TABLET in 1 BOTTLE (71335-2106-7)
71335-2106-8 71335-2106 HUMAN PRESCRIPTION DRUG OXYCODONE AND ACETAMINOPHEN Oxycodone and Acetaminophen TABLET ORAL 20240531 N/A ANDA ANDA207419 Bryant Ranch Prepack ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 10 mg/1 75 TABLET in 1 BOTTLE (71335-2106-8)
71335-2106-9 71335-2106 HUMAN PRESCRIPTION DRUG OXYCODONE AND ACETAMINOPHEN Oxycodone and Acetaminophen TABLET ORAL 20240531 N/A ANDA ANDA207419 Bryant Ranch Prepack ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 10 mg/1 100 TABLET in 1 BOTTLE (71335-2106-9)
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)
31722-951-01 31722-951 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; 10 mg/1 100 TABLET in 1 BOTTLE (31722-951-01)
31722-951-05 31722-951 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; 10 mg/1 500 TABLET in 1 BOTTLE (31722-951-05)
63629-8888-5 63629-8888 HUMAN PRESCRIPTION DRUG OXYCODONE AND ACETAMINOPHEN Oxycodone and Acetaminophen TABLET ORAL 20211217 N/A ANDA ANDA207419 Bryant Ranch Prepack ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 5 mg/1 90 TABLET in 1 BOTTLE (63629-8888-5)
63629-8888-6 63629-8888 HUMAN PRESCRIPTION DRUG OXYCODONE AND ACETAMINOPHEN Oxycodone and Acetaminophen TABLET ORAL 20220621 N/A ANDA ANDA207419 Bryant Ranch Prepack ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 5 mg/1 120 TABLET in 1 BOTTLE (63629-8888-6)
71205-329-10 71205-329 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone and Acetaminophen TABLET ORAL 20191223 N/A ANDA ANDA207419 Proficient Rx LP ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 5 mg/1 10 TABLET in 1 BOTTLE (71205-329-10)
71205-329-28 71205-329 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone and Acetaminophen TABLET ORAL 20220829 N/A ANDA ANDA207419 Proficient Rx LP ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 5 mg/1 28 TABLET in 1 BOTTLE (71205-329-28)
71205-329-30 71205-329 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone and Acetaminophen TABLET ORAL 20190901 N/A ANDA ANDA207419 Proficient Rx LP ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 5 mg/1 30 TABLET in 1 BOTTLE (71205-329-30)
71205-329-60 71205-329 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone and Acetaminophen TABLET ORAL 20190901 N/A ANDA ANDA207419 Proficient Rx LP ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 5 mg/1 60 TABLET in 1 BOTTLE (71205-329-60)
71205-329-90 71205-329 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone and Acetaminophen TABLET ORAL 20190901 N/A ANDA ANDA207419 Proficient Rx LP ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 5 mg/1 90 TABLET in 1 BOTTLE (71205-329-90)
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