NDC 52544-283 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 52544-283 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA020701 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | GM |
| Marketing Start Date | 1997-05-13 |
| Marketing End Date | 2015-02-28 |