NDC 63629-4022 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 63629-4022 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA077050 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2009-07-30 |
| Marketing End Date | 2011-04-01 |
| Marketing Category | ANDA |
| Application Number | ANDA077050 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2009-07-30 |
| Marketing End Date | 2011-04-01 |