NDC 0093-5350 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0093-5350 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA077284 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2008-05-30 |
| Marketing End Date | 2013-01-31 |
| Marketing Category | ANDA |
| Application Number | ANDA077284 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2008-05-30 |
| Marketing End Date | 2013-01-31 |