NDC 61894-001 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 61894-001 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA020184 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2014-10-10 |
| Marketing End Date | 2014-11-18 |
| Marketing Category | NDA |
| Application Number | NDA020184 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2014-10-10 |
| Marketing End Date | 2017-03-01 |