NDC 0074-0541 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0074-0541 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA065003 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2016-06-20 |
| Marketing End Date | 2018-04-27 |