NDC 0004-6416 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0004-6416 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA020067 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1994-10-14 |
| Marketing End Date | 2018-07-31 |