NDC 50991-578 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 50991-578 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA077727 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2006-11-06 |
| Marketing End Date | 2019-01-01 |
| Marketing Category | ANDA |
| Application Number | ANDA077727 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2015-03-03 |
| Marketing End Date | 2015-10-21 |