NDC 0591-0338 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0591-0338 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA075185 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1998-11-13 |
| Marketing End Date | 2015-02-28 |
| Marketing Category | ANDA |
| Application Number | ANDA075185 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1998-11-13 |
| Marketing End Date | 2015-02-28 |
| Marketing Category | ANDA |
| Application Number | ANDA075185 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1998-11-13 |
| Marketing End Date | 2015-02-28 |