NDC 76218-1215 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 76218-1215 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA017604 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2014-07-14 |
| Marketing End Date | 2015-11-05 |