NDC 0093-8397 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0093-8397 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA075126 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2000-01-14 |
| Marketing End Date | 2013-03-31 |