NDC 76045-011 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 76045-011 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA019034 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2016-12-16 |
| Marketing End Date | 2018-02-08 |