NDC 68084-889 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 68084-889 | 
| Marketing Category | / | 
| Marketing Category | ANDA | 
| Application Number | ANDA078179 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 2016-04-13 | 
| Marketing End Date | 2018-06-30 | 
| Marketing Category | ANDA | 
| Application Number | ANDA078179 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 2016-04-13 | 
| Marketing End Date | 2018-06-30 |