NDC 51655-929 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 51655-929 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA074056 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2016-06-20 |
| Inactivation Date | 2020-01-31 |