NDC 76218-0708 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 76218-0708 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA022370 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2012-03-14 |
| Marketing End Date | 2015-10-30 |
| Marketing Category | NDA |
| Application Number | NDA022370 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2012-03-14 |
| Marketing End Date | 2015-10-30 |