NDC 0440-7610 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0440-7610 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA089160 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2010-04-22 |
| Inactivation Date | 2020-01-31 |