NDC 61894-002 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 61894-002 | 
| 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 |