NDC 60505-4651 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 60505-4651 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA078317 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2018-02-09 |
| Marketing End Date | 2018-02-22 |