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=ANDA040777"
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
50268-644-15 50268-644 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone and Acetaminophen TABLET ORAL 20180709 N/A ANDA ANDA040777 AvPAK ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 5 mg/1 50 BLISTER PACK in 1 BOX (50268-644-15) / 1 TABLET in 1 BLISTER PACK (50268-644-11)
53746-203-01 53746-203 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone and Acetaminophen TABLET ORAL 20071127 N/A ANDA ANDA040777 Amneal Pharmaceuticals of New York LLC ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 5 mg/1 100 TABLET in 1 BOTTLE (53746-203-01)
53746-203-05 53746-203 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone and Acetaminophen TABLET ORAL 20071127 N/A ANDA ANDA040777 Amneal Pharmaceuticals of New York LLC ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 5 mg/1 500 TABLET in 1 BOTTLE (53746-203-05)
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