NDC 65862-035 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 65862-035 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA065308 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2006-03-29 |
| Marketing End Date | 2016-01-31 |
| Marketing Category | ANDA |
| Application Number | ANDA065308 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2006-03-29 |
| Marketing End Date | 2016-01-31 |
| Marketing Category | ANDA |
| Application Number | ANDA065308 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2011-05-01 |
| Marketing End Date | 2013-01-22 |