NDC 0062-5351 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0062-5351 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA019641 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1988-06-27 |
| Marketing End Date | 2014-03-31 |