NDC 0004-6202 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0004-6202 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA018164 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1980-09-04 |
| Marketing End Date | 2017-01-31 |