| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 59762-0401-1 | 59762-0401 | HUMAN PRESCRIPTION DRUG | Sucralfate | Sucralfate | TABLET | ORAL | 20170925 | N/A | NDA AUTHORIZED GENERIC | NDA018333 | Greenstone LLC | SUCRALFATE | 1 g/1 | 100 TABLET in 1 BOTTLE (59762-0401-1) |
| 59762-0401-5 | 59762-0401 | HUMAN PRESCRIPTION DRUG | Sucralfate | Sucralfate | TABLET | ORAL | 20170925 | N/A | NDA AUTHORIZED GENERIC | NDA018333 | Greenstone LLC | SUCRALFATE | 1 g/1 | 500 TABLET in 1 BOTTLE (59762-0401-5) |
| 51655-475-52 | 51655-475 | HUMAN PRESCRIPTION DRUG | Sucralfate | Sucralfate | TABLET | ORAL | 20201118 | N/A | NDA AUTHORIZED GENERIC | NDA018333 | Northwind Pharmaceuticals, LLC | SUCRALFATE | 1 g/1 | 30 TABLET in 1 BOTTLE, PLASTIC (51655-475-52) |