NDC 0832-1008 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0832-1008 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA073229 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1991-10-29 |
| Marketing End Date | 2005-12-30 |
| Marketing Category | ANDA |
| Application Number | ANDA073229 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1991-10-29 |
| Marketing End Date | 2016-05-31 |