NDC 68084-900 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 68084-900 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA077653 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2015-02-15 |
| Marketing End Date | 2016-04-26 |
| Marketing Category | ANDA |
| Application Number | ANDA077653 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2015-02-15 |
| Marketing End Date | 2018-11-30 |
| Marketing Category | ANDA |
| Application Number | ANDA077653 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2015-09-01 |
| Marketing End Date | 2018-11-30 |
| Marketing Category | ANDA |
| Application Number | ANDA077653 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2015-09-01 |
| Marketing End Date | 2018-11-30 |