NDC 16252-508 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 16252-508 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA076685 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2006-12-20 |
| Marketing End Date | 2013-01-31 |
| Marketing Category | ANDA |
| Application Number | ANDA076685 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2006-12-20 |
| Marketing End Date | 2013-01-31 |
| Marketing Category | ANDA |
| Application Number | ANDA076685 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2006-12-20 |
| Marketing End Date | 2013-01-31 |
| Marketing Category | ANDA |
| Application Number | ANDA076685 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2006-12-20 |
| Marketing End Date | 2013-01-31 |