NDC 50090-2081 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 50090-2081 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA077095 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2015-10-08 |
| Marketing End Date | 2018-07-31 |
| Marketing Category | ANDA |
| Application Number | ANDA077095 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2015-10-08 |
| Marketing End Date | 2018-04-30 |
| Marketing Category | ANDA |
| Application Number | ANDA077095 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2015-10-08 |
| Marketing End Date | 2018-07-31 |
| Marketing Category | ANDA |
| Application Number | ANDA077095 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2015-10-08 |
| Marketing End Date | 2018-03-31 |
| Marketing Category | ANDA |
| Application Number | ANDA077095 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2015-10-08 |
| Marketing End Date | 2018-07-31 |