NDC 0006-3514 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0006-3514 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA050587 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1985-11-26 |
| Marketing End Date | 2017-05-01 |