NDC 54436-075 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 54436-075 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA204824 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2013-10-11 |
| Marketing End Date | 2016-09-30 |
| Marketing Category | NDA |
| Application Number | NDA204824 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2013-10-11 |
| Marketing End Date | 2016-09-30 |
| Marketing Category | NDA |
| Application Number | NDA204824 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2013-10-11 |
| Marketing End Date | 2016-09-30 |