NDC 0591-5382 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0591-5382 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA084276 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1987-11-01 |
| Marketing End Date | 2013-09-30 |
| Marketing Category | ANDA |
| Application Number | ANDA084276 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1987-11-01 |
| Marketing End Date | 2013-09-30 |