NDC 0093-0661 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0093-0661 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA073419 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 1992-05-01 |
| Marketing End Date | 2018-10-31 |