NDC 60951-310 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 60951-310 |
| Marketing Category | / |
| Marketing Category | NDA AUTHORIZED GENERIC |
| Application Number | NDA007337 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1994-05-20 |
| Marketing End Date | 2014-01-31 |