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=ANDA207418"
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
31722-918-01 31722-918 HUMAN PRESCRIPTION DRUG Oxycodone Hydrochloride Oxycodone Hydrochloride TABLET ORAL 20170808 N/A ANDA ANDA207418 Camber Pharmaceuticals Inc OXYCODONE HYDROCHLORIDE 30 mg/1 100 TABLET in 1 BOTTLE (31722-918-01)
31722-918-05 31722-918 HUMAN PRESCRIPTION DRUG Oxycodone Hydrochloride Oxycodone Hydrochloride TABLET ORAL 20170808 N/A ANDA ANDA207418 Camber Pharmaceuticals Inc OXYCODONE HYDROCHLORIDE 30 mg/1 500 TABLET in 1 BOTTLE (31722-918-05)
72865-128-01 72865-128 HUMAN PRESCRIPTION DRUG Oxycodone Hydrochloride Oxycodone Hydrochloride TABLET ORAL 20200225 N/A ANDA ANDA207418 XLCare Pharmaceuticals, Inc OXYCODONE HYDROCHLORIDE 15 mg/1 100 TABLET in 1 BOTTLE (72865-128-01)
31722-485-01 31722-485 HUMAN PRESCRIPTION DRUG Oxycodone Hydrochloride Oxycodone Hydrochloride TABLET ORAL 20251114 N/A ANDA ANDA207418 Camber Pharmaceuticals Inc OXYCODONE HYDROCHLORIDE 10 mg/1 100 TABLET in 1 BOTTLE (31722-485-01)
31722-485-05 31722-485 HUMAN PRESCRIPTION DRUG Oxycodone Hydrochloride Oxycodone Hydrochloride TABLET ORAL 20251114 N/A ANDA ANDA207418 Camber Pharmaceuticals Inc OXYCODONE HYDROCHLORIDE 10 mg/1 500 TABLET in 1 BOTTLE (31722-485-05)
31722-484-01 31722-484 HUMAN PRESCRIPTION DRUG Oxycodone Hydrochloride Oxycodone Hydrochloride TABLET ORAL 20251114 N/A ANDA ANDA207418 Camber Pharmaceuticals Inc OXYCODONE HYDROCHLORIDE 5 mg/1 100 TABLET in 1 BOTTLE (31722-484-01)
31722-484-05 31722-484 HUMAN PRESCRIPTION DRUG Oxycodone Hydrochloride Oxycodone Hydrochloride TABLET ORAL 20251114 N/A ANDA ANDA207418 Camber Pharmaceuticals Inc OXYCODONE HYDROCHLORIDE 5 mg/1 500 TABLET in 1 BOTTLE (31722-484-05)
31722-917-01 31722-917 HUMAN PRESCRIPTION DRUG Oxycodone Hydrochloride Oxycodone Hydrochloride TABLET ORAL 20170808 N/A ANDA ANDA207418 Camber Pharmaceuticals Inc OXYCODONE HYDROCHLORIDE 15 mg/1 100 TABLET in 1 BOTTLE (31722-917-01)
31722-917-05 31722-917 HUMAN PRESCRIPTION DRUG Oxycodone Hydrochloride Oxycodone Hydrochloride TABLET ORAL 20170808 N/A ANDA ANDA207418 Camber Pharmaceuticals Inc OXYCODONE HYDROCHLORIDE 15 mg/1 500 TABLET in 1 BOTTLE (31722-917-05)
72865-128-05 72865-128 HUMAN PRESCRIPTION DRUG Oxycodone Hydrochloride Oxycodone Hydrochloride TABLET ORAL 20200225 N/A ANDA ANDA207418 XLCare Pharmaceuticals, Inc OXYCODONE HYDROCHLORIDE 15 mg/1 500 TABLET in 1 BOTTLE (72865-128-05)
72865-129-01 72865-129 HUMAN PRESCRIPTION DRUG Oxycodone Hydrochloride Oxycodone Hydrochloride TABLET ORAL 20200225 N/A ANDA ANDA207418 XLCare Pharmaceuticals, Inc OXYCODONE HYDROCHLORIDE 30 mg/1 100 TABLET in 1 BOTTLE (72865-129-01)
72865-129-05 72865-129 HUMAN PRESCRIPTION DRUG Oxycodone Hydrochloride Oxycodone Hydrochloride TABLET ORAL 20200225 N/A ANDA ANDA207418 XLCare Pharmaceuticals, Inc OXYCODONE HYDROCHLORIDE 30 mg/1 500 TABLET in 1 BOTTLE (72865-129-05)
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