NDC 55111-736 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 55111-736 |
| Marketing Category | / |
| Marketing Category | NDA authorized generic |
| Application Number | NDA020132 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2008-11-01 |
| Marketing End Date | 2011-01-28 |