NDC 0591-0388 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0591-0388 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA081079 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1991-08-30 |
| Marketing End Date | 2015-08-31 |