NDC 0955-1035 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0955-1035 |
| Marketing Category | / |
| Marketing Category | NDA AUTHORIZED GENERIC |
| Application Number | NDA014399 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2014-04-01 |
| Marketing End Date | 2016-04-30 |