NDC 0548-3011 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0548-3011 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA086283 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1979-08-07 |
| Marketing End Date | 2009-12-15 |