NDC 67457-382 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 67457-382 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA075440 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2014-03-01 |
| Marketing End Date | 2017-04-27 |
| Marketing Category | ANDA |
| Application Number | ANDA075440 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2013-04-23 |
| Marketing End Date | 2017-04-27 |