NDC 68084-053 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 68084-053 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA074984 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2013-04-19 |
| Marketing End Date | 2018-09-30 |
| Marketing Category | ANDA |
| Application Number | ANDA074984 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2013-03-14 |
| Marketing End Date | 2018-08-31 |
| Marketing Category | ANDA |
| Application Number | ANDA074984 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2013-03-10 |
| Marketing End Date | 2018-08-31 |
| Marketing Category | ANDA |
| Application Number | ANDA074984 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2013-04-19 |
| Marketing End Date | 2018-09-30 |