NDC 25021-661 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 25021-661 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA090316 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2012-03-19 |
| Marketing End Date | 2016-09-01 |
| Marketing Category | ANDA |
| Application Number | ANDA090316 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2012-03-19 |
| Marketing End Date | 2017-07-01 |