NDC 61919-981 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 61919-981 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA204446 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2016-05-27 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | ANDA |
| Application Number | ANDA204446 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2016-05-27 |
| Inactivation Date | 2020-01-31 |