NDC 0781-3333 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0781-3333 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA201002 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2011-06-08 |
| Marketing End Date | 2011-06-08 |
| Marketing Category | ANDA |
| Application Number | ANDA201002 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2011-06-08 |
| Marketing End Date | 2011-06-08 |