NDC 50436-2995 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 50436-2995 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA202045 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2016-09-01 |
| Marketing End Date | 2017-12-31 |