NDC 62756-580 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 62756-580 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA077058 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2014-12-15 |
| Marketing End Date | 2017-11-30 |