NDC 60429-122 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 60429-122 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA090174 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2013-06-12 |
| Marketing End Date | 2018-01-31 |
| Marketing Category | ANDA |
| Application Number | ANDA090174 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2013-06-12 |
| Marketing End Date | 2018-12-31 |