NDC 69543-101 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 69543-101 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA062713 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2015-06-02 |
| Marketing End Date | 2017-11-30 |
| Marketing Category | ANDA |
| Application Number | ANDA062713 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2015-06-02 |
| Marketing End Date | 2018-07-31 |