NDC 48102-006 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 48102-006 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA060764 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | GM |
| Marketing Start Date | 2011-07-15 |
| Marketing End Date | 2013-06-14 |