NDC 0781-3203 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0781-3203 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA203563 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2020-04-10 |
| Marketing End Date | 2015-04-27 |