NDC 72835-004 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 72835-004 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA200675 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2019-06-03 |
| Marketing End Date | 2019-06-04 |