NDC 52544-279 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 52544-279 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA073594 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1997-04-01 |
| Marketing End Date | 2018-06-30 |