NDC 50090-1218 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 50090-1218 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA076265 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2014-11-28 |
| Marketing End Date | 2018-07-31 |
| Marketing Category | ANDA |
| Application Number | ANDA076265 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2014-11-28 |
| Marketing End Date | 2018-07-31 |
| Marketing Category | ANDA |
| Application Number | ANDA076265 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2014-11-28 |
| Marketing End Date | 2018-07-31 |