NDC 16252-618 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 16252-618 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA079167 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2016-08-31 |
| Marketing End Date | 2018-10-31 |
| Marketing Category | ANDA |
| Application Number | ANDA079167 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2016-08-23 |
| Marketing End Date | 2018-10-31 |
| Marketing Category | ANDA |
| Application Number | ANDA079167 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2016-05-02 |
| Marketing End Date | 2018-10-31 |