NDC 68084-890 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 68084-890 |
| Marketing Category | / |
| Marketing Category | NDA authorized generic |
| Application Number | NDA021121 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2016-05-12 |
| Marketing End Date | 2017-10-31 |
| Marketing Category | NDA authorized generic |
| Application Number | NDA021121 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2016-05-12 |
| Marketing End Date | 2017-10-31 |