NDC 61314-015 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 61314-015 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA078222 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2008-03-31 |
| Marketing End Date | 2018-10-31 |
| Marketing Category | ANDA |
| Application Number | ANDA078222 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2008-03-31 |
| Marketing End Date | 2018-08-31 |