NDC 0006-3551 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0006-3551 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA062756 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1987-01-08 |
| Marketing End Date | 2016-05-31 |