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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
68682-101-10 | 68682-101 | HUMAN PRESCRIPTION DRUG | Pentoxifylline | Pentoxifylline | TABLET, EXTENDED RELEASE | ORAL | 20140822 | N/A | ANDA | ANDA075028 | Oceanside Pharmaceuticals | PENTOXIFYLLINE | 400 mg/1 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68682-101-10) |
68682-101-50 | 68682-101 | HUMAN PRESCRIPTION DRUG | Pentoxifylline | Pentoxifylline | TABLET, EXTENDED RELEASE | ORAL | 20140822 | N/A | ANDA | ANDA075028 | Oceanside Pharmaceuticals | PENTOXIFYLLINE | 400 mg/1 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68682-101-50) |