NDC 63481-229 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 63481-229 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA022239 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2015-06-08 |
| Marketing End Date | 2017-05-31 |
| Marketing Category | NDA |
| Application Number | NDA022239 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2015-06-08 |
| Marketing End Date | 2017-05-31 |
| Marketing Category | NDA |
| Application Number | NDA022239 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2015-06-08 |
| Marketing End Date | 2017-05-31 |
| Marketing Category | NDA |
| Application Number | NDA022239 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2015-06-08 |
| Marketing End Date | 2017-05-31 |