NDC 16590-014 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 16590-014 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA065271 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2005-09-11 |
| Inactivation Date | 2019-11-13 |
| Marketing Category | ANDA |
| Application Number | ANDA065271 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2005-09-11 |
| Marketing End Date | 2012-06-12 |
| Marketing Category | ANDA |
| Application Number | ANDA065271 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2005-09-11 |
| Inactivation Date | 2019-11-13 |