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
72865-113-05 72865-113 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; 2.5 mg/1 500 TABLET in 1 BOTTLE (72865-113-05)
71205-347-12 71205-347 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone and Acetaminophen TABLET ORAL 20191101 N/A ANDA ANDA207419 Proficient Rx LP ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 10 mg/1 12 TABLET in 1 BOTTLE (71205-347-12)
71205-347-15 71205-347 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone and Acetaminophen TABLET ORAL 20191101 N/A ANDA ANDA207419 Proficient Rx LP ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 10 mg/1 15 TABLET in 1 BOTTLE (71205-347-15)
71205-347-20 71205-347 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone and Acetaminophen TABLET ORAL 20191101 N/A ANDA ANDA207419 Proficient Rx LP ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 10 mg/1 20 TABLET in 1 BOTTLE (71205-347-20)
71205-347-30 71205-347 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone and Acetaminophen TABLET ORAL 20191101 N/A ANDA ANDA207419 Proficient Rx LP ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 10 mg/1 30 TABLET in 1 BOTTLE (71205-347-30)
71205-347-60 71205-347 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone and Acetaminophen TABLET ORAL 20191101 N/A ANDA ANDA207419 Proficient Rx LP ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 10 mg/1 60 TABLET in 1 BOTTLE (71205-347-60)
71205-347-90 71205-347 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone and Acetaminophen TABLET ORAL 20191101 N/A ANDA ANDA207419 Proficient Rx LP ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 10 mg/1 90 TABLET in 1 BOTTLE (71205-347-90)
31722-194-01 31722-194 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; 10 mg/1 100 TABLET in 1 BOTTLE (31722-194-01)
31722-194-05 31722-194 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; 10 mg/1 500 TABLET in 1 BOTTLE (31722-194-05)
71335-1953-7 71335-1953 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone and Acetaminophen TABLET ORAL 20221013 N/A ANDA ANDA207419 Bryant Ranch Prepack ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 7.5 mg/1 28 TABLET in 1 BOTTLE (71335-1953-7)
71335-1953-8 71335-1953 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone and Acetaminophen TABLET ORAL 20221013 N/A ANDA ANDA207419 Bryant Ranch Prepack ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 7.5 mg/1 168 TABLET in 1 BOTTLE (71335-1953-8)
71335-1953-9 71335-1953 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone and Acetaminophen TABLET ORAL 20221013 N/A ANDA ANDA207419 Bryant Ranch Prepack ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 7.5 mg/1 20 TABLET in 1 BOTTLE (71335-1953-9)
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)
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