NDC 16252-529 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 16252-529 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA076939 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2017-12-28 |
| Marketing End Date | 2018-07-31 |
| Marketing Category | ANDA |
| Application Number | ANDA076939 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2012-02-16 |
| Marketing End Date | 2015-11-06 |
| Marketing Category | ANDA |
| Application Number | ANDA076939 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2007-12-28 |
| Marketing End Date | 2015-11-06 |
| Marketing Category | ANDA |
| Application Number | ANDA076939 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2007-12-28 |
| Marketing End Date | 2018-06-30 |