NDC 60758-910 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 60758-910 |
| Marketing Category | / |
| Marketing Category | NDA AUTHORIZED GENERIC |
| Application Number | NDA019404 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 1997-05-29 |
| Marketing End Date | 2017-09-21 |