NDC 61314-294 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 61314-294 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA088771 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2004-07-01 |
| Marketing End Date | 2018-08-31 |