NDC 68462-232 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 68462-232 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA091672 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2014-10-31 |
| Marketing End Date | 2018-07-01 |
| Marketing Category | ANDA |
| Application Number | ANDA091672 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2014-10-31 |
| Marketing End Date | 2018-07-01 |
| Marketing Category | ANDA |
| Application Number | ANDA091672 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2014-10-31 |
| Marketing End Date | 2018-08-01 |
| Marketing Category | ANDA |
| Application Number | ANDA091672 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2014-10-31 |
| Marketing End Date | 2018-07-01 |