NDC 0591-3775 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0591-3775 |
| Marketing Category | / |
| Marketing Category | NDA AUTHORIZED GENERIC |
| Application Number | NDA020702 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1996-12-17 |
| Marketing End Date | 2015-10-31 |
| Marketing Category | NDA AUTHORIZED GENERIC |
| Application Number | NDA020702 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1996-12-17 |
| Marketing End Date | 2015-10-31 |
| Marketing Category | NDA AUTHORIZED GENERIC |
| Application Number | NDA020702 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1996-12-17 |
| Marketing End Date | 2015-10-31 |
| Marketing Category | NDA AUTHORIZED GENERIC |
| Application Number | NDA020702 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1996-12-17 |
| Marketing End Date | 2015-10-31 |