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=ANDA091490"
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
71335-1422-4 71335-1422 HUMAN PRESCRIPTION DRUG Oxycodone Hydrochloride Oxycodone Hydrochloride TABLET ORAL 20191021 N/A ANDA ANDA091490 Bryant Ranch Prepack OXYCODONE HYDROCHLORIDE 10 mg/1 90 TABLET in 1 BOTTLE (71335-1422-4)
71335-1422-5 71335-1422 HUMAN PRESCRIPTION DRUG Oxycodone Hydrochloride Oxycodone Hydrochloride TABLET ORAL 20240709 N/A ANDA ANDA091490 Bryant Ranch Prepack OXYCODONE HYDROCHLORIDE 10 mg/1 40 TABLET in 1 BOTTLE (71335-1422-5)
71335-1422-6 71335-1422 HUMAN PRESCRIPTION DRUG Oxycodone Hydrochloride Oxycodone Hydrochloride TABLET ORAL 20240709 N/A ANDA ANDA091490 Bryant Ranch Prepack OXYCODONE HYDROCHLORIDE 10 mg/1 28 TABLET in 1 BOTTLE (71335-1422-6)
68071-2899-4 68071-2899 HUMAN PRESCRIPTION DRUG Oxycodone Hydrochloride Oxycodone Hydrochloride TABLET ORAL 20221208 N/A ANDA ANDA091490 NuCare Pharmaceuticals,Inc. OXYCODONE HYDROCHLORIDE 5 mg/1 4 TABLET in 1 BOTTLE, PLASTIC (68071-2899-4)
68071-2899-6 68071-2899 HUMAN PRESCRIPTION DRUG Oxycodone Hydrochloride Oxycodone Hydrochloride TABLET ORAL 20221208 N/A ANDA ANDA091490 NuCare Pharmaceuticals,Inc. OXYCODONE HYDROCHLORIDE 5 mg/1 6 TABLET in 1 BOTTLE, PLASTIC (68071-2899-6)
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