NDC 0093-7252 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0093-7252 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA076447 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2005-09-01 |
| Marketing End Date | 2012-08-31 |
| Marketing Category | ANDA |
| Application Number | ANDA076447 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2005-09-01 |
| Marketing End Date | 2012-08-31 |