NDC 52544-552 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 52544-552 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA070687 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1987-01-29 |
| Marketing End Date | 2009-02-28 |
| Marketing Category | ANDA |
| Application Number | ANDA070687 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1987-01-29 |
| Marketing End Date | 2017-12-31 |