NDC 45861-062 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 45861-062 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA203818 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2015-08-13 |
| Marketing End Date | 2018-01-01 |