NDC 68084-182 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 68084-182 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA077397 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2010-12-08 |
| Marketing End Date | 2019-01-31 |
| Marketing Category | ANDA |
| Application Number | ANDA077397 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2010-12-01 |
| Marketing End Date | 2019-01-31 |