NDC 25021-222 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 25021-222 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA203551 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2013-07-01 |
| Marketing End Date | 2017-03-31 |
| Marketing Category | NDA |
| Application Number | NDA203551 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2013-07-01 |
| Marketing End Date | 2017-03-31 |
| Marketing Category | NDA |
| Application Number | NDA203551 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2013-07-01 |
| Marketing End Date | 2017-03-31 |