NDC 55111-608 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 55111-608 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA090723 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2014-06-18 |
| Marketing End Date | 2016-06-17 |
| Marketing Category | ANDA |
| Application Number | ANDA090723 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2014-06-18 |
| Marketing End Date | 2016-06-17 |
| Marketing Category | ANDA |
| Application Number | ANDA090723 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2014-06-18 |
| Marketing End Date | 2016-06-17 |
| Marketing Category | ANDA |
| Application Number | ANDA090723 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2014-06-18 |
| Marketing End Date | 2016-06-17 |