NDC 0548-3369 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0548-3369 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA072076 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2001-06-01 |
| Marketing End Date | 2013-01-10 |