NDC 36000-029 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 36000-029 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA078024 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2012-10-23 |
| Marketing End Date | 2018-05-09 |