NDC 67425-999 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 67425-999 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA021664 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2010-09-20 |
| Marketing End Date | 2017-12-29 |
| Marketing Category | NDA |
| Application Number | NDA021664 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2010-09-20 |
| Marketing End Date | 2017-12-29 |
| Marketing Category | NDA |
| Application Number | NDA021664 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2010-09-20 |
| Marketing End Date | 2017-12-29 |