NDC 0172-2985 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0172-2985 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA062500 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2010-03-24 |
| Marketing End Date | 2011-02-28 |
| Marketing Category | ANDA |
| Application Number | ANDA062500 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2010-03-24 |
| Marketing End Date | 2011-02-28 |
| Marketing Category | ANDA |
| Application Number | ANDA062500 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2010-03-24 |
| Marketing End Date | 2011-02-28 |
| Marketing Category | ANDA |
| Application Number | ANDA062500 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2010-03-24 |
| Marketing End Date | 2011-02-28 |