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=ANDA074425"
符合检索条件的记录共 6 条，共 1 页，当前第 1 页 ，可点击列名称排序
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
71335-2586-3 71335-2586 HUMAN PRESCRIPTION DRUG Pentoxifylline Pentoxifylline TABLET, EXTENDED RELEASE ORAL 20250407 N/A ANDA ANDA074425 Bryant Ranch Prepack PENTOXIFYLLINE 400 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2586-3)
71335-2586-2 71335-2586 HUMAN PRESCRIPTION DRUG Pentoxifylline Pentoxifylline TABLET, EXTENDED RELEASE ORAL 20250407 N/A ANDA ANDA074425 Bryant Ranch Prepack PENTOXIFYLLINE 400 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2586-2)
71335-2586-1 71335-2586 HUMAN PRESCRIPTION DRUG Pentoxifylline Pentoxifylline TABLET, EXTENDED RELEASE ORAL 20250407 N/A ANDA ANDA074425 Bryant Ranch Prepack PENTOXIFYLLINE 400 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2586-1)
16571-856-01 16571-856 HUMAN PRESCRIPTION DRUG Pentoxifylline Pentoxifylline TABLET, EXTENDED RELEASE ORAL 20240611 N/A ANDA ANDA074425 Rising Pharma Holdings, Inc. PENTOXIFYLLINE 400 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (16571-856-01)
16571-856-50 16571-856 HUMAN PRESCRIPTION DRUG Pentoxifylline Pentoxifylline TABLET, EXTENDED RELEASE ORAL 20240611 N/A ANDA ANDA074425 Rising Pharma Holdings, Inc. PENTOXIFYLLINE 400 mg/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (16571-856-50)
16571-856-90 16571-856 HUMAN PRESCRIPTION DRUG Pentoxifylline Pentoxifylline TABLET, EXTENDED RELEASE ORAL 20240611 N/A ANDA ANDA074425 Rising Pharma Holdings, Inc. PENTOXIFYLLINE 400 mg/1 1 BLISTER PACK in 1 CARTON (16571-856-90) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
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