NDC 42291-392 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 42291-392 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA076262 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2013-06-18 |
| Marketing End Date | 2018-11-19 |
| Marketing Category | ANDA |
| Application Number | ANDA076262 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2013-06-18 |
| Marketing End Date | 2018-11-19 |
| Marketing Category | ANDA |
| Application Number | ANDA076262 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2013-10-28 |
| Marketing End Date | 2015-02-24 |