NDC 25021-778 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 25021-778 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA091136 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2013-05-31 |
| Marketing End Date | 2017-01-31 |
| Marketing Category | ANDA |
| Application Number | ANDA091136 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2010-12-01 |
| Marketing End Date | 2017-02-01 |