NDC 0548-1240 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0548-1240 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA083722 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2003-04-18 |
| Marketing End Date | 2009-09-01 |