| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 69067-010-15 | 69067-010 | HUMAN PRESCRIPTION DRUG | Lactulose | Lactulose | SOLUTION | ORAL | 20180921 | N/A | ANDA | ANDA074712 | Foxland Pharmaceuticals, Inc. | LACTULOSE | 10 g/10g | 15 POUCH in 1 CARTON (69067-010-15) / 10 g in 1 POUCH |
| 66220-729-30 | 66220-729 | HUMAN PRESCRIPTION DRUG | KRISTALOSE | lactulose | POWDER, FOR SOLUTION | ORAL | 20120120 | N/A | ANDA | ANDA074712 | Cumberland Pharmaceuticals Inc. | LACTULOSE | 20 g/20g | 30 POUCH in 1 CARTON (66220-729-30) / 20 g in 1 POUCH (66220-729-01) |
| 66220-719-30 | 66220-719 | HUMAN PRESCRIPTION DRUG | KRISTALOSE | lactulose | POWDER, FOR SOLUTION | ORAL | 20120120 | N/A | ANDA | ANDA074712 | Cumberland Pharmaceuticals Inc. | LACTULOSE | 10 g/10g | 30 POUCH in 1 CARTON (66220-719-30) / 10 g in 1 POUCH (66220-719-01) |