NDC 42291-320 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 42291-320 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA040133 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2012-12-31 |
| Marketing End Date | 2015-11-04 |
| Marketing Category | ANDA |
| Application Number | ANDA040133 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2012-02-29 |
| Marketing End Date | 2015-11-04 |