NDC 52544-936 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 52544-936 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA018985 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2002-12-07 |
| Marketing End Date | 2016-05-31 |