NDC 58118-0303 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 58118-0303 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA020064 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2011-05-25 |
| Marketing End Date | 2016-08-25 |
| Marketing Category | ANDA |
| Application Number | ANDA020064 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2011-05-25 |
| Marketing End Date | 2016-08-25 |
| Marketing Category | ANDA |
| Application Number | ANDA020064 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2011-05-25 |
| Marketing End Date | 2016-08-25 |