NDC 50268-101 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 50268-101 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA065509 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2014-03-26 |
| Marketing End Date | 2017-02-27 |
| Marketing Category | ANDA |
| Application Number | ANDA065509 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2014-09-19 |
| Marketing End Date | 2017-02-27 |