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=ANDA202677"
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
47781-229-01 47781-229 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone and Acetaminophen TABLET ORAL 20120117 N/A ANDA ANDA202677 Alvogen, Inc. ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 7.5 mg/1 100 TABLET in 1 BOTTLE (47781-229-01)
35356-801-30 35356-801 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone and Acetaminophen TABLET ORAL 20130910 20260430 ANDA ANDA202677 Quality Care Products, LLC ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 10 mg/1 30 TABLET in 1 BOTTLE (35356-801-30)
35356-801-60 35356-801 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone and Acetaminophen TABLET ORAL 20130910 20260430 ANDA ANDA202677 Quality Care Products, LLC ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 10 mg/1 60 TABLET in 1 BOTTLE (35356-801-60)
35356-801-90 35356-801 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone and Acetaminophen TABLET ORAL 20130910 20260430 ANDA ANDA202677 Quality Care Products, LLC ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 10 mg/1 90 TABLET in 1 BOTTLE (35356-801-90)
47781-229-05 47781-229 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone and Acetaminophen TABLET ORAL 20120117 N/A ANDA ANDA202677 Alvogen, Inc. ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 7.5 mg/1 500 TABLET in 1 BOTTLE (47781-229-05)
68084-710-01 68084-710 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone and Acetaminophen TABLET ORAL 20140604 N/A ANDA ANDA202677 American Health Packaging ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 10 mg/1 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-710-01) / 1 TABLET in 1 BLISTER PACK (68084-710-11)
71335-0216-0 71335-0216 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone and Acetaminophen TABLET ORAL 20160725 N/A ANDA ANDA202677 Bryant Ranch Prepack ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 5 mg/1 25 TABLET in 1 BOTTLE (71335-0216-0)
71335-0216-1 71335-0216 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone and Acetaminophen TABLET ORAL 20160725 N/A ANDA ANDA202677 Bryant Ranch Prepack ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 5 mg/1 10 TABLET in 1 BOTTLE (71335-0216-1)
71335-0216-2 71335-0216 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone and Acetaminophen TABLET ORAL 20160725 N/A ANDA ANDA202677 Bryant Ranch Prepack ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 5 mg/1 120 TABLET in 1 BOTTLE (71335-0216-2)
71335-0216-3 71335-0216 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone and Acetaminophen TABLET ORAL 20160725 N/A ANDA ANDA202677 Bryant Ranch Prepack ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 5 mg/1 28 TABLET in 1 BOTTLE (71335-0216-3)
71335-0216-4 71335-0216 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone and Acetaminophen TABLET ORAL 20160725 N/A ANDA ANDA202677 Bryant Ranch Prepack ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 5 mg/1 12 TABLET in 1 BOTTLE (71335-0216-4)
71335-0216-5 71335-0216 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone and Acetaminophen TABLET ORAL 20160725 N/A ANDA ANDA202677 Bryant Ranch Prepack ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 5 mg/1 40 TABLET in 1 BOTTLE (71335-0216-5)
71335-0216-6 71335-0216 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone and Acetaminophen TABLET ORAL 20160725 N/A ANDA ANDA202677 Bryant Ranch Prepack ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 5 mg/1 30 TABLET in 1 BOTTLE (71335-0216-6)
71335-0216-7 71335-0216 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone and Acetaminophen TABLET ORAL 20160725 N/A ANDA ANDA202677 Bryant Ranch Prepack ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 5 mg/1 90 TABLET in 1 BOTTLE (71335-0216-7)
71335-0216-8 71335-0216 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone and Acetaminophen TABLET ORAL 20160725 N/A ANDA ANDA202677 Bryant Ranch Prepack ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 5 mg/1 60 TABLET in 1 BOTTLE (71335-0216-8)
71335-0216-9 71335-0216 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone and Acetaminophen TABLET ORAL 20160725 N/A ANDA ANDA202677 Bryant Ranch Prepack ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 5 mg/1 84 TABLET in 1 BOTTLE (71335-0216-9)
60760-899-30 60760-899 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone and Acetaminophen TABLET ORAL 20250821 N/A ANDA ANDA202677 ST. MARY'S MEDICAL PARK PHARMACY ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 10 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (60760-899-30)
60760-899-60 60760-899 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone and Acetaminophen TABLET ORAL 20250821 N/A ANDA ANDA202677 ST. MARY'S MEDICAL PARK PHARMACY ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 10 mg/1 60 TABLET in 1 BOTTLE, PLASTIC (60760-899-60)
60760-899-90 60760-899 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone and Acetaminophen TABLET ORAL 20250821 N/A ANDA ANDA202677 ST. MARY'S MEDICAL PARK PHARMACY ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 10 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (60760-899-90)
47781-230-01 47781-230 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone and Acetaminophen TABLET ORAL 20120117 N/A ANDA ANDA202677 Alvogen, Inc. ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 10 mg/1 100 TABLET in 1 BOTTLE (47781-230-01)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2025 Drugfuture->U.S. FDA National Drug Code DataBase