NDC 55700-381 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 55700-381 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA079087 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2016-03-03 |
| Marketing End Date | 2016-12-31 |
| Marketing Category | ANDA |
| Application Number | ANDA079087 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2016-03-03 |
| Marketing End Date | 2018-11-02 |